6-<<(1,1-dimethylethoxy)carbonyl>amino>-2-<1-<<(benzyloxy)carbonyl>methyl>-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-3-yl>hexanoic acid benzyl ester

Base Information

Chemical Name:6-<<(1,1-dimethylethoxy)carbonyl>amino>-2-<1-<<(benzyloxy)carbonyl>methyl>-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-3-yl>hexanoic acid benzyl ester
CAS No.:158387-21-4
Molecular Formula:C₃₇H₄₅N₃O₇
Molecular Weight:643.78
Hs Code.:

Synonyms:6-<<(1,1-dimethylethoxy)carbonyl>amino>-2-<1-<<(benzyloxy)carbonyl>methyl>-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-3-yl>hexanoic acid benzyl ester

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Chemical Property of 6-<<(1,1-dimethylethoxy)carbonyl>amino>-2-<1-<<(benzyloxy)carbonyl>methyl>-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-3-yl>hexanoic acid benzyl ester

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Technology Process of 6-<<(1,1-dimethylethoxy)carbonyl>amino>-2-<1-<<(benzyloxy)carbonyl>methyl>-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-3-yl>hexanoic acid benzyl ester

There total 1 articles about 6-<<(1,1-dimethylethoxy)carbonyl>amino>-2-<1-<<(benzyloxy)carbonyl>methyl>-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-3-yl>hexanoic acid benzyl 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: 90.0%

: 100-39-0
benzyl bromide

: 97878-50-7
(S)-6-tert-Butoxycarbonylamino-2-((S)-1-carboxymethyl-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b]azepin-3-ylamino)-hexanoic acid

: 158387-21-4
6-<<(1,1-dimethylethoxy)carbonyl>amino>-2-<1-<<(benzyloxy)carbonyl>methyl>-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-3-yl>hexanoic acid benzyl ester

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; for 48h; Ambient temperature;
DOI:10.1021/jm00038a011

Reference yield: 90.0%

: 158387-21-4
6-<<(1,1-dimethylethoxy)carbonyl>amino>-2-<1-<<(benzyloxy)carbonyl>methyl>-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-3-yl>hexanoic acid benzyl ester

: 6-amino-2-<1-<<(benzyloxy)carbonyl>methyl>-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-3-yl>hexanoic acid benzyl ester

Guidance literature:: With hydrogenchloride; In ethyl acetate; for 16h;
DOI:10.1021/jm00038a011

Reference yield:

: 158387-21-4
6-<<(1,1-dimethylethoxy)carbonyl>amino>-2-<1-<<(benzyloxy)carbonyl>methyl>-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-3-yl>hexanoic acid benzyl ester

: 158387-23-6
2-<<1-(carboxymethyl)-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-3-yl>amino>-6-<<5-<5-chloro-1-methyl-2-(3-pyridinyl)-1H-idol-3-yl>pentanoyl>amino>hexanoic acid dibenzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / HCl / ethyl acetate / 16 h

2: 52 percent / triethylamine, 1-<3-(dimethylamino)propyl>-2-ethylcarbodiimide hydrochloride (EDCl) / CH₂Cl₂ / 16 h

With hydrogenchloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; ethyl acetate;
DOI:10.1021/jm00038a011