Benzyloxycarbonylamino-thioacetic acid S-[(S)-2-tert-butoxycarbonylamino-3-(4-methoxy-2-oxo-2,5-dihydro-pyrrol-1-yl)-3-oxo-propyl] ester

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Chemical Name:Benzyloxycarbonylamino-thioacetic acid S-[(S)-2-tert-butoxycarbonylamino-3-(4-methoxy-2-oxo-2,5-dihydro-pyrrol-1-yl)-3-oxo-propyl] ester
CAS No.:180415-73-0
Molecular Formula:C₂₃H₂₉N₃O₈S
Molecular Weight:507.565
Hs Code.:

Synonyms:Benzyloxycarbonylamino-thioacetic acid S-[(S)-2-tert-butoxycarbonylamino-3-(4-methoxy-2-oxo-2,5-dihydro-pyrrol-1-yl)-3-oxo-propyl] ester

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Chemical Property of Benzyloxycarbonylamino-thioacetic acid S-[(S)-2-tert-butoxycarbonylamino-3-(4-methoxy-2-oxo-2,5-dihydro-pyrrol-1-yl)-3-oxo-propyl] ester

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Technology Process of Benzyloxycarbonylamino-thioacetic acid S-[(S)-2-tert-butoxycarbonylamino-3-(4-methoxy-2-oxo-2,5-dihydro-pyrrol-1-yl)-3-oxo-propyl] ester

There total 5 articles about Benzyloxycarbonylamino-thioacetic acid S-[(S)-2-tert-butoxycarbonylamino-3-(4-methoxy-2-oxo-2,5-dihydro-pyrrol-1-yl)-3-oxo-propyl] 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: 73.0%

: 2899-60-7
Cbz-Gly-ONSuc

: 180415-72-9
[(S)-1-Mercaptomethyl-2-(4-methoxy-2-oxo-2,5-dihydro-pyrrol-1-yl)-2-oxo-ethyl]-carbamic acid tert-butyl ester

: 180415-73-0
Benzyloxycarbonylamino-thioacetic acid S-[(S)-2-tert-butoxycarbonylamino-3-(4-methoxy-2-oxo-2,5-dihydro-pyrrol-1-yl)-3-oxo-propyl] ester

Guidance literature:: With triethylamine; In tetrahydrofuran;
DOI:10.1016/S0960-894X(96)00270-3

Reference yield:

: 1138-80-3
N-(Benzyloxycarbonyl)glycine

: 180415-73-0
Benzyloxycarbonylamino-thioacetic acid S-[(S)-2-tert-butoxycarbonylamino-3-(4-methoxy-2-oxo-2,5-dihydro-pyrrol-1-yl)-3-oxo-propyl] ester

Guidance literature:: Multi-step reaction with 2 steps

2: 73 percent / Et₃N / tetrahydrofuran

With triethylamine; In tetrahydrofuran;
DOI:10.1016/S0960-894X(96)00270-3

Reference yield:

: 58290-35-0
N-tert-butyloxycarbonyl-S-p-methoxybenzyl-D-cysteine

: 180415-73-0
Benzyloxycarbonylamino-thioacetic acid S-[(S)-2-tert-butoxycarbonylamino-3-(4-methoxy-2-oxo-2,5-dihydro-pyrrol-1-yl)-3-oxo-propyl] ester

Guidance literature:: Multi-step reaction with 4 steps

1: DCC / tetrahydrofuran

2: 1.) NaH / 1.) THF, reflux, 30 min, 2.) THF, 0 deg C

3: 1.) Hg(CF₃CO₂)2, 2.) H₂S / 1.) AcOH, 2.) AcOH, 10 min

4: 73 percent / Et₃N / tetrahydrofuran

With Hg(II) trifluoroacetate; hydrogen sulfide; sodium hydride; triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran;
DOI:10.1016/S0960-894X(96)00270-3