(S)-2-Benzyloxycarbonylamino-4-phenylsulfanyl-pent-4-enoic acid methyl ester

Base Information

Chemical Name:(S)-2-Benzyloxycarbonylamino-4-phenylsulfanyl-pent-4-enoic acid methyl ester
CAS No.:203920-13-2
Molecular Formula:C₂₀H₂₁NO₄S
Molecular Weight:371.457
Hs Code.:

Synonyms:(S)-2-Benzyloxycarbonylamino-4-phenylsulfanyl-pent-4-enoic acid methyl ester

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Chemical Property of (S)-2-Benzyloxycarbonylamino-4-phenylsulfanyl-pent-4-enoic acid methyl ester

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Technology Process of (S)-2-Benzyloxycarbonylamino-4-phenylsulfanyl-pent-4-enoic acid methyl ester

There total 4 articles about (S)-2-Benzyloxycarbonylamino-4-phenylsulfanyl-pent-4-enoic 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: 98.0%

: 501-53-1,94274-21-2
benzyl chloroformate

: 203920-12-1
(S)-2-Amino-4-phenylsulfanyl-pent-4-enoic acid methyl ester

: 203920-13-2
(S)-2-Benzyloxycarbonylamino-4-phenylsulfanyl-pent-4-enoic acid methyl ester

Guidance literature:: With pyridine; In dichloromethane; for 4h; Ambient temperature;
DOI:10.1021/jo972133h

Reference yield:

: 15893-06-8
1-Chlor-2-phenylthio-2-propen

: 203920-13-2
(S)-2-Benzyloxycarbonylamino-4-phenylsulfanyl-pent-4-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 1) n-BuLi / 1) THF, hexane, -78 deg C, 10 min, 2) THF, hexane, -60 deg C, 4 h; -60 deg C to room temperature, 12 h

2: 79 percent / CF₃CO₂H / tetrahydrofuran / 4 h / Ambient temperature

3: 98 percent / pyridine / CH₂Cl₂ / 4 h / Ambient temperature

With pyridine; n-butyllithium; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jo972133h

Reference yield:

: 931-59-9
benzenesulfenyl chloride

: 203920-13-2
(S)-2-Benzyloxycarbonylamino-4-phenylsulfanyl-pent-4-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: tetrahydrofuran / 0.5 h / -30 - -20 °C

2: 1) n-BuLi / 1) THF, hexane, -78 deg C, 10 min, 2) THF, hexane, -60 deg C, 4 h; -60 deg C to room temperature, 12 h

3: 79 percent / CF₃CO₂H / tetrahydrofuran / 4 h / Ambient temperature

4: 98 percent / pyridine / CH₂Cl₂ / 4 h / Ambient temperature

With pyridine; n-butyllithium; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jo972133h