(S)-benzyl 2-(2-((S)-1-(benzyloxy)-3-methyl-1-oxobutan-2-ylcarbamoyl)-3-methylphenylcarbamoyl)pyrrolidine-1-carboxylate

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Chemical Name:(S)-benzyl 2-(2-((S)-1-(benzyloxy)-3-methyl-1-oxobutan-2-ylcarbamoyl)-3-methylphenylcarbamoyl)pyrrolidine-1-carboxylate
CAS No.:1337570-18-9
Molecular Formula:C₃₃H₃₇N₃O₆
Molecular Weight:571.673
Hs Code.:

Synonyms:(S)-benzyl 2-(2-((S)-1-(benzyloxy)-3-methyl-1-oxobutan-2-ylcarbamoyl)-3-methylphenylcarbamoyl)pyrrolidine-1-carboxylate

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Chemical Property of (S)-benzyl 2-(2-((S)-1-(benzyloxy)-3-methyl-1-oxobutan-2-ylcarbamoyl)-3-methylphenylcarbamoyl)pyrrolidine-1-carboxylate

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Technology Process of (S)-benzyl 2-(2-((S)-1-(benzyloxy)-3-methyl-1-oxobutan-2-ylcarbamoyl)-3-methylphenylcarbamoyl)pyrrolidine-1-carboxylate

There total 3 articles about (S)-benzyl 2-(2-((S)-1-(benzyloxy)-3-methyl-1-oxobutan-2-ylcarbamoyl)-3-methylphenylcarbamoyl)pyrrolidine-1-carboxylate 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: 48.0%

: 1337570-17-8
(S)-benzyl 2-(2-amino-6-methylbenzamido)-3-methylbutanoate

: 1148-11-4
N-Benzyloxycarbonyl-L-proline

: 1337570-18-9
(S)-benzyl 2-(2-((S)-1-(benzyloxy)-3-methyl-1-oxobutan-2-ylcarbamoyl)-3-methylphenylcarbamoyl)pyrrolidine-1-carboxylate

Guidance literature:: With pyridine; trichlorophosphate; at -10 - -5 ℃; Inert atmosphere;
DOI:10.1021/ol202284n

Reference yield:

: 20877-81-0
5-methyl-1H-benzo[d][1,3]oxazine-2,4-dione

: 1337570-18-9
(S)-benzyl 2-(2-((S)-1-(benzyloxy)-3-methyl-1-oxobutan-2-ylcarbamoyl)-3-methylphenylcarbamoyl)pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / ethyl acetate / 10 h / Reflux; Inert atmosphere

2: pyridine; trichlorophosphate / -10 - -5 °C / Inert atmosphere

With pyridine; triethylamine; trichlorophosphate; In ethyl acetate;
DOI:10.1021/ol202284n

Reference yield:

: 2462-34-2
L-valine benzyl ester hydrochloride

: 1337570-18-9
(S)-benzyl 2-(2-((S)-1-(benzyloxy)-3-methyl-1-oxobutan-2-ylcarbamoyl)-3-methylphenylcarbamoyl)pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / ethyl acetate / 10 h / Reflux; Inert atmosphere

2: pyridine; trichlorophosphate / -10 - -5 °C / Inert atmosphere

With pyridine; triethylamine; trichlorophosphate; In ethyl acetate;
DOI:10.1021/ol202284n