Tag: M.W:100-200

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.30448-16-9,7-Methyl-1H-indole-3-carboxylic acid,as a common compound, the synthetic route is as follows.

The bispyridine ester amine compound (200 mg, 0.99 mmol) in Example 1 and 7-methyl-1H-indole-3-carboxylic acid (170 mg, 0.99 mmol) were dissolved in DMF (5 ml), DCC (230 mg, 1.09 mmol) was added to the solution, and then the mixture was stirred at 80 C. for 8 hours. After the reaction was completed, the product was washed and filtered to yield a target compound as a white solid (30 ml, 7%) by chromatography (methanol:dichloromethane=1:30)., 30448-16-9

30448-16-9 7-Methyl-1H-indole-3-carboxylic acid 14810856, aindole-building-block compound, is more and more widely used in various fields.

Reference£º
Patent; KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY; US2009/258876; (2009); A1;,
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.50820-65-0,Methyl 1H-indole-6-carboxylate,as a common compound, the synthetic route is as follows.,50820-65-0

To a solution of methyl 1H-indole-6-carboxylate (17.5 g, 99.9 mmol, 1.0 eq) in i-PrOH (200 mL) was added cyclopent-2-en-1-one (16.4 g, 199.8 mmol, 16.7 mL, 2.0 eq) and SnCl2*2H2O (2.25 g, 9.99 mmol, 831.8 muL, 0.1 eq) under N2. After addition, the mixture was stirred at room temperature for 16 h. The reaction mixture was concentrated and diluted with DCM (250 mL). The organic layer was separated and washed with H2O (200 mL), brine (200 mL), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure to give a residue. The residue was purified by column chromatography (SiO2) to give compound 03-4-1 (22.4 g, 79percent yield).1H NMR (CDCl3, 400 MHz): delta 8.38 (s, 1 H) 8.17 (s, 1 H) 7.84 (d, J=8.8 Hz, 1 H) 7.66 (d, J=8.8 Hz, 1 H) 7.19 (d, J=2.01 Hz, 1 H) 3.97 (s, 3 H) 3.74-3.77 (m, 1 H) 2.77-2.83 (m, 1 H) 2.58-2.59 (m, 1 H) 2.39-2.48 (m, 3 H) 2.15-2.17 (m, 1 H).

50820-65-0 Methyl 1H-indole-6-carboxylate 639844, aindole-building-block compound, is more and more widely used in various fields.

Reference£º
Patent; KYRAS THERAPEUTICS, INC.; VACCA, Joseph P.; LI, Dansu; (587 pag.)WO2017/96045; (2017); A1;,
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.15317-58-5,1H-Indole-3-carbohydrazide,as a common compound, the synthetic route is as follows.

General procedure: 1H-Indole-3-carboxylate methylester 2 (1.0 mmol-equiv.) was refluxed with hydrazine hydrate(12.5 g, 0.25 M) in appropriate ethanol (30 mL) for 2 h. The progressof the reaction was monitored by TLC. After cooling the reactionmixture to room temperature, the mixtures were filtered to givewhite solid crude products without purification. Next, indolehydrazide(3, 1.0 mmol) in ethanol (30 mL) was added dropwiseinto the appropriate aldehyde (1.5 mmol-equiv.) and a few drops ofpropionic acid; the mixture was stirred and refluxed for 2.5 h. Aftercooling, the precipitates were filtered and washed several times bymethanol to yield the crystal substances 4aeu., 15317-58-5

As the paragraph descriping shows that 15317-58-5 is playing an increasingly important role.

Reference£º
Article; Ju, Zhiran; Su, Mingzhi; Hong, Jongki; La Kim, Eun; Moon, Hyung Ryong; Chung, Hae Young; Kim, Suhkmann; Jung, Jee H.; European Journal of Medicinal Chemistry; vol. 180; (2019); p. 86 – 98;,
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

1196-70-9, 1H-Indole-6-carbaldehyde is a indole-building-block compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

General procedure: 6-(4-Hydroxy-3-methoxyphenyl)hexa-5-ene-2,4-dione (20 mg, 85 mumol) and B2O3 (11 mg, 0.16 mmol) were dissolved in 0.4 mL of AcOEt. To the stirring mixture at 80C was added a solution of 3-hydroxy-2-methoxybenzaldehyde (16 mg, 0.11 mmol) and tributyl borate (25 muL, 93 mumol) in 0.7 mL of AcOEt. After the reaction mixture was stirred at 80C for 2 hours, n-butylamine (10 muL, 0.10 mmol) was added with additional stirring for 1 hour. The reaction mixture was treated with a solution of 1 N HCl and saturated brine (1:1 mixture), stirred at 50C for 5 min, and neutralized by saturated NaHCO3 aqueous solution. The organic layer was directly chromatographed on silica gel (hexane/AcOEt system or CHCl3/MeOH system) to yield the title compound as a solid (10.2 mg) in 32% yield.

1196-70-9, 1196-70-9 1H-Indole-6-carbaldehyde 2773435, aindole-building-block compound, is more and more widely used in various fields.

Reference£º
Article; Okuda, Michiaki; Hijikuro, Ichiro; Fujita, Yuki; Teruya, Takayuki; Kawakami, Hirochika; Takahashi, Takashi; Sugimoto, Hachiro; Bioorganic and Medicinal Chemistry Letters; vol. 26; 20; (2016); p. 5024 – 5028;,
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.5416-80-8,2-Methyl-1H-indole-3-carbaldehyde,as a common compound, the synthetic route is as follows.

INTERMEDIATE 9 – PREPARATION OF 3-(5-Chloro-1 H-indol-3-yl)propan-1-amine. To a solution of 3-(3-Azidopropyl)-5-chloro-1 H-indole (0.299 g; 1.27 mmol) in THF (9 mL) were added triphenylphosphine (0.354 g; 1.34 mmol) and water (0.6 mL). The reaction mixture was stirred at room temperature for 22 hours and was then concentrated under reduced pressure. The residue was dissolved in dichloromethane (10 mL) and 10 mL of 6N hydrochloric acid were added. After separation, the aqueous layer was further extracted with dichloromethane (2×10 mL) and the pH was adjusted to 14 with an aqueous solution of sodium hydroxide 6N. This basic solution was extracted dichloromethane (3×20 mL) and the combined organic layer was dried over magnesium sulphate, and evaporated to afford 0.089 g (34%) of 3-(5-Chloro-1 H-indol-3-yl)propan-1 -amine as a white solid.ESI/APCI(+): 209 (M+H); ESI/APCI(-): 207 (M-H).

5416-80-8, 5416-80-8 2-Methyl-1H-indole-3-carbaldehyde 73166, aindole-building-block compound, is more and more widely used in various fields.

Reference£º
Patent; KATHOLIEKE UNIVERSITEIT LEUVEN, K.U. LEUVEN R&D; REMYND; GRIFFIOEN, Gerard; VAN DOOREN, Tom; ROJAS DE LA PARRA, Veronica; MARCHAND, Arnaud; ALLASIA, Sara; KILONDA, Amuri; CHALTIN, Patrick; WO2012/80220; (2012); A1;,
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

3770-50-1, Ethyl indole-2-carboxylate is a indole-building-block compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

To a solution of ethyl 1H-indole-2-carboxylate (2 mmol) in dry DMF (10 mL) was added NBS (2 mmol). The resulting mixture was stirred at room temperature under nitrogen gas for 12 h. Crushed ice was added into the reaction mixture. White precipitate appeared was collected under vacuum suction, washed with cold water, dried, and re-crystallized from ethanol to get pure product (1) (0.49 g, 90%); mp146-148 C; FTIR (KBr, cm-1) numax: 3377, 3297, 1686,1573, 1515, 740, 642; 1H NMR (400 MHz, CDCl3): delta =9.28 (s, 1H, NH), 7.67 (m, 1H, Ar-H), 7.40 (m, 2H, Ar-H),7.25 (m, 1H, Ar-H), 4.49 (q, J = 7.12 Hz, 2H,COOCH2CH3), 1.47 (t, J = 7.08 Hz, 3H, COOCH2CH3); 13C NMR (100MHz, CDCl3): delta = 161.16 (C,COOCH2CH3), 135.41 (C, C-2), 128.01 (C, C-7a), 126.57(CH, C-4), 121.47 (CH, C-5), 121.33 (CH, C-6), 112.06 (CH, C-7), 98.31 (C-Br, C-3), 61.54 (CH2, COOCH2CH3),14.36 (CH3, COOCH2CH3); ESI-MS (m/z): [M+Na]+Calcd for C11H10BrNO2: 266.98; Found: 289.98., 3770-50-1

As the paragraph descriping shows that 3770-50-1 is playing an increasingly important role.

Reference£º
Article; Singh, Amanjot; Verma, Raman K.; Kuhad, Anurag; Mall, Rajiv; Medicinal Chemistry Research; vol. 26; 4; (2017); p. 745 – 759;,
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

10242-02-1, 5-Methyl-1H-indole-3-carboxylic acid is a indole-building-block compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

General procedure: Following the above procedure, the crude reaction mixture was diluted with MeOH and cooled to 0C. Then SOCl2 (36 muL, 0.5 mmol) was added and stirred for 3 h at room temperature. Additional MeOH was added and the reaction mixture was heated to reflux for 6 h. The resulting mixture was quenched with H2O and extracted with EtOAc (3x). The combined organic layers were dried over MgSO4 and concentrated under reduced pressure. The resulting crude residue was purified by preparative TLC (hexane:EtOAc = 7:3) to afford the desired products 5a-b.

10242-02-1, 10242-02-1 5-Methyl-1H-indole-3-carboxylic acid 18385291, aindole-building-block compound, is more and more widely used in various fields.

Reference£º
Article; Yoo, Woo-Jin; Nguyen, Thanh V. Q.; Guiteras Capdevila, Montse; Kobayashi, Shu; Heterocycles; vol. 90; 2; (2015); p. 1196 – 1204;,
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.6960-42-5,7-Nitro-1H-indole,as a common compound, the synthetic route is as follows.

6960-42-5, General procedure: First, a solution of a benzoheterocycle (an indole, a benzofuran or abenzo[b]thiophene) (0.3 mmol), an arylsulfonyl hydrazide (0.8 mmol),Cu(OTf)2 (0.2 mmol), HOAc (2 mL) and H2O (0.1 mL) in toluene(1 mL) was stirred at 110 C for 8 h under air. Second, the reaction mixture was quenched with water (10 mL) and extracted with EtOAc(3 ¡Á 10 mL). The combined EtOAc extracts were dried over anhydrous MgSO4 and the solvent removed under reduced pressure. The residue was purified by flash column chromatography on silica gel using PE/EtOAc as the eluent.

The synthetic route of 6960-42-5 has been constantly updated, and we look forward to future research findings.

Reference£º
Article; Chen, Lingjuan; Pu, Jiangxin; Liu, Ping; Dai, Bin; Journal of Chemical Research; vol. 42; 9; (2018); p. 456 – 462;,
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

245-08-9, 5H-Pyrido[3,2-b]indole is a indole-building-block compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

o a 250 ml two-necked flask was added delta -carboline (15 g, 89 mmol), 1-bromo-4-iodobenzene,, CuI (1.1 g, 5.79 mmol), 1,10-phenanthroline (2 g, 11.13 mmol), K3PO4 (47 g, 220 mmol)(Dioxane, 300 ml) were put together and refluxed at 80 to 100 C under nitrogen for 24 hours. After the reaction was completed, methylene chloride(MC) and Celite filter. The filtered solution was distilled under reduced pressure, then extracted with MC and distilled waterAll. The extracted MC layer was extracted with MgSO4 and the solvent was removed by distillation under reduced pressure to obtain a yellow solid. This solidThe white solid (2) was isolated (18.7 g, 65%) using the Column Chromatography method., 245-08-9

As the paragraph descriping shows that 245-08-9 is playing an increasingly important role.

Reference£º
Patent; WS Co., Ltd; Koh, Byung Soo; Kim, Kyu Sik; Kwak, Tae Young; Oh, Yu Jin; (36 pag.)KR2015/9205; (2015); A;,
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

15317-58-5, 1H-Indole-3-carbohydrazide is a indole-building-block compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

General procedure: Equimolar quantities of compound 2 (1 mmol) and a substituted carboxylic acid were dissolved in phosphoryl chloride (5 mL) and heated at 80C for 3-6 h, the progress of reaction being monitored by TLC. The reaction mixture was then heated under reduced pressure to allow excess phosphoryl chloride to distill off, and the residue was subjected to flash chromatography on silica gel using 15-25% acetone in petroleum ether as eluent to give the target compounds 3a-m (Table 1).

15317-58-5, The synthetic route of 15317-58-5 has been constantly updated, and we look forward to future research findings.

Reference£º
Article; Zhang, Ming-Zhi; Mulholland, Nick; Beattie, David; Irwin, Dianne; Gu, Yu-Cheng; Chen, Qiong; Yang, Guang-Fu; Clough, John; European Journal of Medicinal Chemistry; vol. 63; (2013); p. 22 – 32;,
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles