(1R,3R)-methyl 1-(3-acetoxyphenyl)-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylate

Base Information

Chemical Name:(1R,3R)-methyl 1-(3-acetoxyphenyl)-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylate
CAS No.:1353844-67-3
Molecular Formula:C₂₁H₂₀N₂O₄
Molecular Weight:364.401
Hs Code.:

Synonyms:(1R,3R)-methyl 1-(3-acetoxyphenyl)-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylate

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Chemical Property of (1R,3R)-methyl 1-(3-acetoxyphenyl)-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylate

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Technology Process of (1R,3R)-methyl 1-(3-acetoxyphenyl)-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylate

There total 3 articles about (1R,3R)-methyl 1-(3-acetoxyphenyl)-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylate 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: 96.0%

: 34231-78-2
3-formylphenyl acetate

: 1353874-70-0
D-tryptophan methyl ester hydrobromide

: 1353844-67-3
(1R,3R)-methyl 1-(3-acetoxyphenyl)-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylate

Guidance literature:: 3-formylphenyl acetate; D-tryptophan methyl ester hydrobromide; In isopropyl alcohol; for 2h; Reflux;

In nitromethane; toluene; for 12h; optical yield given as %de; diastereoselective reaction; Reflux;
DOI:10.1016/j.tetasy.2011.10.011

Reference yield: 95.0%

: 34231-78-2
3-formylphenyl acetate

: 14907-27-8,5619-09-0,7524-52-9,26988-71-6,41222-70-2,67557-19-1,109492-62-8
(R)-(+)-tryptophan methyl ester hydrochloride

: 1353844-67-3
(1R,3R)-methyl 1-(3-acetoxyphenyl)-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylate

Guidance literature:: 3-formylphenyl acetate; (R)-(+)-tryptophan methyl ester hydrochloride; In isopropyl alcohol; for 2h; Reflux;

In nitromethane; toluene; for 18h; optical yield given as %de; diastereoselective reaction; Reflux;
DOI:10.1016/j.tetasy.2011.10.011

Reference yield:

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

: 1353844-67-3
(1R,3R)-methyl 1-(3-acetoxyphenyl)-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrogen bromide / ethyl acetate / 1.25 h / 0 °C

2.1: isopropyl alcohol / 2 h / Reflux

2.2: 12 h / Reflux

With hydrogen bromide; In ethyl acetate; isopropyl alcohol; 2.1: Pictet-Spengler reaction;
DOI:10.1016/j.tetasy.2011.10.011