Some tips on 1008-07-7

As the paragraph descriping shows that 1008-07-7 is playing an increasingly important role.

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.1008-07-7,7-Chloro-1H-indole-3-carbaldehyde,as a common compound, the synthetic route is as follows.

To a stirring solution of 7-chloro-?H-indole-3-carbaldehyde SM1 (200 mg, 1.lmmol) in MeOH (10m1),was added TMSCN (168mg, 1.5mmol), NH3 (gas) was chargedinto the mixture at 0C. The reaction mixture stirred at 45C for 3 h. After consumption of the starting material (by TLC), the reaction mixture concentrated under reduced pressure to obtain crude product, which washed with ether to afford compound 1 (200mg, 88%). TLC:30% EA/PE (Rf: 0.3). LC-MS: m/z = 206[(M+1)], 1008-07-7

As the paragraph descriping shows that 1008-07-7 is playing an increasingly important role.

Reference:
Patent; ABBVIE INC.; KESICKI, Edward A.; WANG, Ce; PATANE, Michael A.; KLUGE, Arthur F.; VAN DRIE, JR., John H.; (121 pag.)WO2016/44777; (2016); 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