(S)-N-((S)-1-tert-Butoxycarbonyl-2-phenyl-ethyl)-3-[5-(4-thiocarbamoyl-phenyl)-pentanoylamino]-succinamic acid tert-butyl ester

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Chemical Name:(S)-N-((S)-1-tert-Butoxycarbonyl-2-phenyl-ethyl)-3-[5-(4-thiocarbamoyl-phenyl)-pentanoylamino]-succinamic acid tert-butyl ester
CAS No.:145643-12-5
Molecular Formula:C₃₃H₄₅N₃O₆S
Molecular Weight:611.803
Hs Code.:

Synonyms:(S)-N-((S)-1-tert-Butoxycarbonyl-2-phenyl-ethyl)-3-[5-(4-thiocarbamoyl-phenyl)-pentanoylamino]-succinamic acid tert-butyl ester

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Chemical Property of (S)-N-((S)-1-tert-Butoxycarbonyl-2-phenyl-ethyl)-3-[5-(4-thiocarbamoyl-phenyl)-pentanoylamino]-succinamic acid tert-butyl ester

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Technology Process of (S)-N-((S)-1-tert-Butoxycarbonyl-2-phenyl-ethyl)-3-[5-(4-thiocarbamoyl-phenyl)-pentanoylamino]-succinamic acid tert-butyl ester

There total 5 articles about (S)-N-((S)-1-tert-Butoxycarbonyl-2-phenyl-ethyl)-3-[5-(4-thiocarbamoyl-phenyl)-pentanoylamino]-succinamic 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: 100.0%

: 145643-11-4
5-(p-cyanophenyl)pentanoyl-(S)-aspartyl(O-tert-butyl)-(S)-phenylalanine(O-tert-butyl)

: 145643-12-5
(S)-N-((S)-1-tert-Butoxycarbonyl-2-phenyl-ethyl)-3-[5-(4-thiocarbamoyl-phenyl)-pentanoylamino]-succinamic acid tert-butyl ester

Guidance literature:: With pyridine; hydrogen sulfide; triethylamine; at 23 ℃; for 24h;
DOI:10.1021/jm00065a003

Reference yield:

: 591-80-0
pent-4-enoic acid

: 145643-12-5
(S)-N-((S)-1-tert-Butoxycarbonyl-2-phenyl-ethyl)-3-[5-(4-thiocarbamoyl-phenyl)-pentanoylamino]-succinamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 54 percent / Bu₄NCl, PPh₃, Pd(OAc)2, KOAc / dimethylformamide / 21 h / 23 °C

2: H₂ / 5percent Pd/CaCO₃ / methanol / 1.2 h / 258.6 Torr

3: 80 percent / N,N-dicyclohexylcarbodiimide (DCC) / CH₂Cl₂ / 20 h / 23 °C

4: 100 percent / H₂S, pyridine , Et₃N / 24 h / 23 °C

With pyridine; palladium diacetate; hydrogen sulfide; tetrabutyl-ammonium chloride; hydrogen; potassium acetate; triethylamine; dicyclohexyl-carbodiimide; triphenylphosphine; Lindlar's catalyst; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm00065a003

Reference yield:

: 623-00-7
4-bromobenzenecarbonitrile

: 145643-12-5
(S)-N-((S)-1-tert-Butoxycarbonyl-2-phenyl-ethyl)-3-[5-(4-thiocarbamoyl-phenyl)-pentanoylamino]-succinamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 54 percent / Bu₄NCl, PPh₃, Pd(OAc)2, KOAc / dimethylformamide / 21 h / 23 °C

2: H₂ / 5percent Pd/CaCO₃ / methanol / 1.2 h / 258.6 Torr

3: 80 percent / N,N-dicyclohexylcarbodiimide (DCC) / CH₂Cl₂ / 20 h / 23 °C

4: 100 percent / H₂S, pyridine , Et₃N / 24 h / 23 °C

With pyridine; palladium diacetate; hydrogen sulfide; tetrabutyl-ammonium chloride; hydrogen; potassium acetate; triethylamine; dicyclohexyl-carbodiimide; triphenylphosphine; Lindlar's catalyst; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm00065a003