3-{3-[2-Benzyloxycarbonylamino-3-(4-thiocarbamoyl-phenyl)-propionylamino]-benzoylamino}-propionic acid benzyl ester

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Chemical Name:3-{3-[2-Benzyloxycarbonylamino-3-(4-thiocarbamoyl-phenyl)-propionylamino]-benzoylamino}-propionic acid benzyl ester
CAS No.:135321-42-5
Molecular Formula:C₃₅H₃₄N₄O₆S
Molecular Weight:638.744
Hs Code.:

Synonyms:3-{3-[2-Benzyloxycarbonylamino-3-(4-thiocarbamoyl-phenyl)-propionylamino]-benzoylamino}-propionic acid benzyl ester

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Chemical Property of 3-{3-[2-Benzyloxycarbonylamino-3-(4-thiocarbamoyl-phenyl)-propionylamino]-benzoylamino}-propionic acid benzyl ester

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Technology Process of 3-{3-[2-Benzyloxycarbonylamino-3-(4-thiocarbamoyl-phenyl)-propionylamino]-benzoylamino}-propionic acid benzyl ester

There total 4 articles about 3-{3-[2-Benzyloxycarbonylamino-3-(4-thiocarbamoyl-phenyl)-propionylamino]-benzoylamino}-propionic acid benzyl 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:

: 135321-41-4
3-{3-[2-Benzyloxycarbonylamino-3-(4-cyano-phenyl)-propionylamino]-benzoylamino}-propionic acid benzyl ester

: 135321-42-5
3-{3-[2-Benzyloxycarbonylamino-3-(4-thiocarbamoyl-phenyl)-propionylamino]-benzoylamino}-propionic acid benzyl ester

Guidance literature:: With hydrogen sulfide; triethylamine; In pyridine; Ambient temperature;
DOI:10.1021/jm00101a017

Reference yield:

: 111331-82-9
3-[(tert-butoxycarbonyl)amino]benzoic acid

: 135321-42-5
3-{3-[2-Benzyloxycarbonylamino-3-(4-thiocarbamoyl-phenyl)-propionylamino]-benzoylamino}-propionic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 1.)2-chloro-4,6-dimethoxy-1,3,5-triazine (CDMT), N-methylmorpholine (NMM), 2.) N-methylmorpholine (NMM) / 1.) CH₂Cl₂, 0 deg C, 3 h, 2.) CH₂Cl₂, RT, 12 h

2: trifluoroacetic acid (TFA) / CH₂Cl₂ / 2 h / Ambient temperature

3: 1.)2-chloro-4,6-dimethoxy-1,3,5-triazine (CDMT), N-methylmorpholine (NMM), 2.) N-methylmorpholine (NMM) / 1.) CH₂Cl₂, 0 deg C, 3 h, 2.) CH₂Cl₂, RT, 12 h

4: H₂S, triethylamine (TEA) / pyridine / Ambient temperature

With 4-methyl-morpholine; 2-chloro-4,6-dimethoxy-1 ,3,5-triazine; hydrogen sulfide; triethylamine; trifluoroacetic acid; In pyridine; dichloromethane;
DOI:10.1021/jm00101a017

Reference yield:

: 135321-13-0
N-[m-(1-t-butoxyformamido)benzoyl]-β-alanine benzyl ester

: 135321-42-5
3-{3-[2-Benzyloxycarbonylamino-3-(4-thiocarbamoyl-phenyl)-propionylamino]-benzoylamino}-propionic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: trifluoroacetic acid (TFA) / CH₂Cl₂ / 2 h / Ambient temperature

2: 1.)2-chloro-4,6-dimethoxy-1,3,5-triazine (CDMT), N-methylmorpholine (NMM), 2.) N-methylmorpholine (NMM) / 1.) CH₂Cl₂, 0 deg C, 3 h, 2.) CH₂Cl₂, RT, 12 h

3: H₂S, triethylamine (TEA) / pyridine / Ambient temperature

With 4-methyl-morpholine; 2-chloro-4,6-dimethoxy-1 ,3,5-triazine; hydrogen sulfide; triethylamine; trifluoroacetic acid; In pyridine; dichloromethane;
DOI:10.1021/jm00101a017