(3R)-2-(tert-butoxycarbonyl)-7-methoxy-3-methyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

Base Information

Chemical Name:(3R)-2-(tert-butoxycarbonyl)-7-methoxy-3-methyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid
CAS No.:1187832-23-0
Molecular Formula:C₁₇H₂₃NO₅
Molecular Weight:321.373
Hs Code.:

Synonyms:(3R)-2-(tert-butoxycarbonyl)-7-methoxy-3-methyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

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Chemical Property of (3R)-2-(tert-butoxycarbonyl)-7-methoxy-3-methyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

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Technology Process of (3R)-2-(tert-butoxycarbonyl)-7-methoxy-3-methyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

There total 4 articles about (3R)-2-(tert-butoxycarbonyl)-7-methoxy-3-methyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid 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: 100.0%

: 1187832-19-4
(3R)-6,8-dibromo-2-(tert-butoxycarbonyl)-7-methoxy-3-methyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

: 1187832-23-0
(3R)-2-(tert-butoxycarbonyl)-7-methoxy-3-methyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

Guidance literature:: With palladium 10% on activated carbon; hydrogen; triethylamine; In methanol; for 1.5h; under 2068.65 Torr;
DOI:10.1021/jm900756t

Reference yield:

: 132616-92-3
O,α-dimethyl-D-tyrosine

: 1187832-23-0
(3R)-2-(tert-butoxycarbonyl)-7-methoxy-3-methyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogenchloride; bromine / water / 5 °C / Inert atmosphere

2.1: trifluoroacetic acid; hydrogen bromide / acetic acid / 17 h / 70 - 80 °C / Inert atmosphere

3.1: triethylamine / N,N-dimethyl-formamide; water / 4 h / 20 °C

3.2: pH 2

4.1: triethylamine; hydrogen / palladium 10% on activated carbon / methanol / 1.5 h / 2828.7 Torr

With hydrogenchloride; hydrogen bromide; hydrogen; bromine; triethylamine; trifluoroacetic acid; palladium 10% on activated carbon; In methanol; water; acetic acid; N,N-dimethyl-formamide;

Reference yield:

: 1187832-17-2
3,5-dibromo-O,α-dimethyl-D-tyrosine

: 1187832-23-0
(3R)-2-(tert-butoxycarbonyl)-7-methoxy-3-methyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: trifluoroacetic acid; hydrogen bromide / acetic acid / 17 h / 70 - 80 °C / Inert atmosphere

2.1: triethylamine / N,N-dimethyl-formamide; water / 4 h / 20 °C

2.2: pH 2

3.1: triethylamine; hydrogen / palladium 10% on activated carbon / methanol / 1.5 h / 2828.7 Torr

With hydrogen bromide; hydrogen; triethylamine; trifluoroacetic acid; palladium 10% on activated carbon; In methanol; water; acetic acid; N,N-dimethyl-formamide;