Simple exploration of 434958-85-7

The synthetic route of 434958-85-7 has been constantly updated, and we look forward to future research findings.

434958-85-7,With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.434958-85-7,N-Boc-5-Hydroxyindole,as a common compound, the synthetic route is as follows.

To a solution of Intermediate 49 (3.00 g, 12.9 mmol, 1.0 eq) in anhydrous MeCN (13 mL) was added a solution of N-bromosuccinimide (2.53 g, 14.2 mmol, 1.1 eq) in anhydrous MeCN (130 mL) dropwise via cannula. After 1.5 h, addition was complete and the reaction mixture was stirred for a further 1 h. The reactionmixture was concentrated in vacuo and purified twice by silica gel chromatography using hexane/CH2CI2 (1 :0-1 .5:1) to yield Intermediate 50 as a white solid (605 mg, 15%).1H NMR (300MHz, DMSO-d5) oH. 9.95 (5, 1H), 7.78-7.91 (m, 1H), 7.61-7.73 (m, 1H), 6.97 (d, J=8.9 Hz, 1H), 6.50-6.59 (m, 1H), 1.54-1.70 (m, 9H).MS (E5) 311.9 (45%, [M-Hfl.

The synthetic route of 434958-85-7 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; KARUS THERAPEUTICS LTD; SHUTTLEWORTH, Stephen Joseph; SILVA, Franck Alexandre; CECIL, Alexander Richard Liam; ALEXANDER, Rikki Peter; GATLAND, Alice Elizabeth; FINNEMORE, Daniel John; (123 pag.)WO2017/29521; (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