(2-{Benzyloxy-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-acetyl]-amino}-3-phenyl-propionylamino)-acetic acid methyl ester

Base Information

Chemical Name:(2-{Benzyloxy-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-acetyl]-amino}-3-phenyl-propionylamino)-acetic acid methyl ester
CAS No.:95204-98-1
Molecular Formula:C₂₉H₂₇N₃O₇
Molecular Weight:529.549
Hs Code.:

Synonyms:(2-{Benzyloxy-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-acetyl]-amino}-3-phenyl-propionylamino)-acetic acid methyl ester

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Chemical Property of (2-{Benzyloxy-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-acetyl]-amino}-3-phenyl-propionylamino)-acetic acid methyl ester

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Technology Process of (2-{Benzyloxy-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-acetyl]-amino}-3-phenyl-propionylamino)-acetic acid methyl ester

There total 4 articles about (2-{Benzyloxy-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-acetyl]-amino}-3-phenyl-propionylamino)-acetic 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: 91.0%

: 6780-38-7
N-phthaloylglycine chloride

: (2-Benzyloxyamino-3-phenyl-propionylamino)-acetic acid methyl ester; hydrochloride

: 95204-98-1
(2-{Benzyloxy-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-acetyl]-amino}-3-phenyl-propionylamino)-acetic acid methyl ester

Guidance literature:: With triethylamine; In N,N-dimethyl-formamide; at -5 ℃; for 24h; oth. N-benzyloxyamino acids;
DOI:10.1246/bcsj.57.2456

Reference yield:

: 54837-24-0
N-benzyloxy-DL-phenylalanine

: 95204-98-1
(2-{Benzyloxy-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-acetyl]-amino}-3-phenyl-propionylamino)-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 88 percent / N,N-dicyclohexylcarbodiimide / tetrahydrofuran / 1) 0 deg C, 1 h, 2) 20 h, refrigerator

2: 85 percent / (C₂H₅)3N / CHCl₃ / 1) 0 deg C, 2 h, 2) room temperature, 24 h

3: 91 percent / (C₂H₅)3N / dimethylformamide / 24 h / -5 °C / oth. N-benzyloxyamino acids

With triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide;
DOI:10.1246/bcsj.57.2456

Reference yield:

: 2-Benzyloxyamino-3-phenyl-propionic acid 2,5-dioxo-pyrrolidin-1-yl ester; hydrochloride

: 95204-98-1
(2-{Benzyloxy-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-acetyl]-amino}-3-phenyl-propionylamino)-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / (C₂H₅)3N / CHCl₃ / 1) 0 deg C, 2 h, 2) room temperature, 24 h

2: 91 percent / (C₂H₅)3N / dimethylformamide / 24 h / -5 °C / oth. N-benzyloxyamino acids

With triethylamine; In chloroform; N,N-dimethyl-formamide;
DOI:10.1246/bcsj.57.2456