(1S,3R)-1-phenyl-2,3,4,9-tetrahydro-1H-pyridine[3,4-b]indole-3-carboxylic acid methyl ester

Base Information

Chemical Name:(1S,3R)-1-phenyl-2,3,4,9-tetrahydro-1H-pyridine[3,4-b]indole-3-carboxylic acid methyl ester
CAS No.:903575-58-6
Molecular Formula:C₁₉H₁₈N₂O₂
Molecular Weight:306.364
Hs Code.:

Synonyms:(1S,3R)-1-phenyl-2,3,4,9-tetrahydro-1H-pyridine[3,4-b]indole-3-carboxylic acid methyl ester

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Chemical Property of (1S,3R)-1-phenyl-2,3,4,9-tetrahydro-1H-pyridine[3,4-b]indole-3-carboxylic acid methyl ester

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Technology Process of (1S,3R)-1-phenyl-2,3,4,9-tetrahydro-1H-pyridine[3,4-b]indole-3-carboxylic acid methyl ester

There total 8 articles about (1S,3R)-1-phenyl-2,3,4,9-tetrahydro-1H-pyridine[3,4-b]indole-3-carboxylic acid methyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 95.0%

: (1S,3R)-methyl 1-phenyl-2-(naphthalen-1-ylmethyl)-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylate

: 903575-58-6
(1S,3R)-1-phenyl-2,3,4,9-tetrahydro-1H-pyridine[3,4-b]indole-3-carboxylic acid methyl ester

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In acetonitrile; at 60 ℃; for 8h; under 798.054 - 836.056 Torr;
DOI:10.1016/j.tetasy.2013.06.006

Reference yield: 82.8%

: 100-52-7
benzaldehyde

: 4299-70-1,7303-49-3,22032-65-1
D-Tryptophan methyl ester

: 104330-95-2
(1R,3R)-1-phenyl-2,3,4,9-tetrahydro-1H-pyridine[3,4-b]indole-3-carboxylic acid methyl ester

: 903575-58-6
(1S,3R)-1-phenyl-2,3,4,9-tetrahydro-1H-pyridine[3,4-b]indole-3-carboxylic acid methyl ester

Guidance literature:: benzaldehyde; D-Tryptophan methyl ester; With titanium(IV) isopropylate; (1R,2S)-2-(N-2'-hydroxy-3'-isopropyl-5'-methoxybenzyl)amino-1,2-diphenylethanol; In tetrahydrofuran; at 0 ℃; for 24h; Inert atmosphere; Molecular sieve;

With trifluoroacetic acid; In tetrahydrofuran; at 0 ℃; for 2h; Inert atmosphere;