{2-[2-(2-benzyloxycarbonylamino-acetylamino)-phenyl]-1-methyl-2-oxo-ethyl}-carbamic acid tert-butyl ester

Base Information

• Chemical Name: {2-[2-(2-benzyloxycarbonylamino-acetylamino)-phenyl]-1-methyl-2-oxo-ethyl}-carbamic acid tert-butyl ester
• CAS No.: 917610-58-3
• Molecular Formula: C₂₄H₂₉N₃O₆
• Molecular Weight: 455.511

Synonyms:{2-[2-(2-benzyloxycarbonylamino-acetylamino)-phenyl]-1-methyl-2-oxo-ethyl}-carbamic acid tert-butyl ester

Chemical Property of {2-[2-(2-benzyloxycarbonylamino-acetylamino)-phenyl]-1-methyl-2-oxo-ethyl}-carbamic acid tert-butyl ester

Chemical Property:

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Technology Process of {2-[2-(2-benzyloxycarbonylamino-acetylamino)-phenyl]-1-methyl-2-oxo-ethyl}-carbamic acid tert-butyl ester

There total 2 articles about {2-[2-(2-benzyloxycarbonylamino-acetylamino)-phenyl]-1-methyl-2-oxo-ethyl}-carbamic acid tert-butyl 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: 71.0%

(S)-2-(tert-butoxycarbonylamino)-1-(2'-aminophenyl)propan-1-one (917610-55-0) + N-(Benzyloxycarbonyl)glycine (1138-80-3) → {2-[2-(2-benzyloxycarbonylamino-acetylamino)-phenyl]-1-methyl-2-oxo-ethyl}-carbamic acid tert-butyl ester (917610-58-3)

Guidance literature:

With dmap; triethylamine; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide;

DOI:10.1021/ol062540s

Reference yield:

<1-(N-tert-butyloxycarbonyl)amino-1-methyl>-N-phenylacetamide (126727-23-9,126787-11-9,68739-47-9) → {2-[2-(2-benzyloxycarbonylamino-acetylamino)-phenyl]-1-methyl-2-oxo-ethyl}-carbamic acid tert-butyl ester (917610-58-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 56 percent / acetonitrile / 48 h / 20 °C / Irradiation

2: 71 percent / DCC; DMAP / CHCl₃ / 12 h / 20 °C

With dmap; dicyclohexyl-carbodiimide; In chloroform; acetonitrile; 1: photo-Fries rearrangement;

DOI:10.1021/jo0614442

Reference yield: 74.0%

{2-[2-(2-benzyloxycarbonylamino-acetylamino)-phenyl]-1-methyl-2-oxo-ethyl}-carbamic acid tert-butyl ester (917610-58-3) → {1-[2-(benzyloxycarbonylamino-methyl)-quinazolin-4-yl]-ethyl}-carbamic acid tert-butyl ester

Guidance literature:

With ammonium formate; at 150 ℃; for 0.15h; under 5171.48 Torr; microwave irradiation;

DOI:10.1021/ol062540s

upstream raw materials:

(S)-2-(tert-butoxycarbonylamino)-1-(2'-aminophenyl)propan-1-one

N-(Benzyloxycarbonyl)glycine

<1-(N-tert-butyloxycarbonyl)amino-1-methyl>-N-phenylacetamide

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