(S)-7-(allyl-tert-butoxycarbonylamino)-7-[2-(3-methoxy-5-vinylbenzyloxy)-phenylcarbamoyl]-heptanoic acid methyl ester

Base Information

Chemical Name:(S)-7-(allyl-tert-butoxycarbonylamino)-7-[2-(3-methoxy-5-vinylbenzyloxy)-phenylcarbamoyl]-heptanoic acid methyl ester
CAS No.:1257657-26-3
Molecular Formula:C₃₃H₄₄N₂O₇
Molecular Weight:580.722
Hs Code.:

Synonyms:(S)-7-(allyl-tert-butoxycarbonylamino)-7-[2-(3-methoxy-5-vinylbenzyloxy)-phenylcarbamoyl]-heptanoic acid methyl ester

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Chemical Property of (S)-7-(allyl-tert-butoxycarbonylamino)-7-[2-(3-methoxy-5-vinylbenzyloxy)-phenylcarbamoyl]-heptanoic acid methyl ester

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Technology Process of (S)-7-(allyl-tert-butoxycarbonylamino)-7-[2-(3-methoxy-5-vinylbenzyloxy)-phenylcarbamoyl]-heptanoic acid methyl ester

There total 3 articles about (S)-7-(allyl-tert-butoxycarbonylamino)-7-[2-(3-methoxy-5-vinylbenzyloxy)-phenylcarbamoyl]-heptanoic 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: 97.0%

: 146651-75-4
tert–butyl (2–aminophenyl)carbamate

: 71590-08-4
5-methoxy-isophthalic acid monomethyl ester

: 1257657-26-3
(S)-7-(allyl-tert-butoxycarbonylamino)-7-[2-(3-methoxy-5-vinylbenzyloxy)-phenylcarbamoyl]-heptanoic acid methyl ester

Guidance literature:: 5-methoxy-isophthalic acid monomethyl ester; With N-ethyl-N,N-diisopropylamine; 3-[(diethoxyphosphinyl)oxy]-1,2,3-benzotriazin-4(3H)-one; In tetrahydrofuran; at 20 ℃; for 0.25h; Cooling with ice; Inert atmosphere;

tert–butyl (2–aminophenyl)carbamate; In tetrahydrofuran; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/jm101092u

Reference yield: 70.0%

: 1257657-18-3
(S)-2-allyloxyoctanedioic acid 8-methyl ester

: 1257657-30-9
5-(acetylaminomethyl)-2-(3-methoxy-5-vinylbenzyloxy)-phenylammonium chloride

: 1257657-26-3
(S)-7-(allyl-tert-butoxycarbonylamino)-7-[2-(3-methoxy-5-vinylbenzyloxy)-phenylcarbamoyl]-heptanoic acid methyl ester

Guidance literature:: (S)-2-allyloxyoctanedioic acid 8-methyl ester; With N-ethyl-N,N-diisopropylamine; 3-[(diethoxyphosphinyl)oxy]-1,2,3-benzotriazin-4(3H)-one; In tetrahydrofuran; at 20 ℃; for 0.25h; Cooling with ice; Inert atmosphere;

5-(acetylaminomethyl)-2-(3-methoxy-5-vinylbenzyloxy)-phenylammonium chloride; In tetrahydrofuran; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/jm101092u

Reference yield: 70.0%

: 1057663-66-7
2-(3-methoxy-5-vinylbenzyloxy)phenylamine

: 1057664-62-6
(S)-2-(allyl-tert-butoxycarbonylamino)octanedioic acid 8-methyl ester

: 1257657-26-3
(S)-7-(allyl-tert-butoxycarbonylamino)-7-[2-(3-methoxy-5-vinylbenzyloxy)-phenylcarbamoyl]-heptanoic acid methyl ester

Guidance literature:: (S)-2-(allyl-tert-butoxycarbonylamino)octanedioic acid 8-methyl ester; With N-ethyl-N,N-diisopropylamine; 3-[(diethoxyphosphinyl)oxy]-1,2,3-benzotriazin-4(3H)-one; In tetrahydrofuran; at 20 ℃; for 0.25h; Cooling with ice; Inert atmosphere;

2-(3-methoxy-5-vinylbenzyloxy)phenylamine; In tetrahydrofuran; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/jm101092u