N-[(2-S-benzyloxycarbonylamino-propanoylamino)methyl] 2-S-methanesulfanyl succinamic acid benzyl ester

Base Information

Chemical Name:N-[(2-S-benzyloxycarbonylamino-propanoylamino)methyl] 2-S-methanesulfanyl succinamic acid benzyl ester
CAS No.:374756-56-6
Molecular Formula:C₂₄H₂₉N₃O₆S
Molecular Weight:487.577
Hs Code.:

Synonyms:N-[(2-S-benzyloxycarbonylamino-propanoylamino)methyl] 2-S-methanesulfanyl succinamic acid benzyl ester

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Chemical Property of N-[(2-S-benzyloxycarbonylamino-propanoylamino)methyl] 2-S-methanesulfanyl succinamic acid benzyl ester

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Technology Process of N-[(2-S-benzyloxycarbonylamino-propanoylamino)methyl] 2-S-methanesulfanyl succinamic acid benzyl ester

There total 5 articles about N-[(2-S-benzyloxycarbonylamino-propanoylamino)methyl] 2-S-methanesulfanyl succinamic 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: 62.0%

: [(1S)-(aminomethyl-carbamoyl)-ethyl]carbamic acid methyl ester

: 374756-25-9
2-S-methanesulfanyl succinic acid 1-benzyl ester

: 374756-56-6
N-[(2-S-benzyloxycarbonylamino-propanoylamino)methyl] 2-S-methanesulfanyl succinamic acid benzyl ester

Guidance literature:: With N-ethylmorpholine;; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 0 ℃; for 1h;
DOI:10.1021/ja003770j

Reference yield:

: 83477-74-1
2-R-hydroxysuccinic acid 1-benzylester

: 374756-56-6
N-[(2-S-benzyloxycarbonylamino-propanoylamino)methyl] 2-S-methanesulfanyl succinamic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: 58 percent / K₃CO₃ / dimethylformamide / 96 h / 20 °C

2.1: 2,6-lutidine; triflic anhydride / CH₂Cl₂ / 4 h / -78 °C

2.2: 76 percent / 15-crown-5 / CH₂Cl₂; dimethylformamide / -78 - 20 °C

3.1: 100 percent / TFA / CH₂Cl₂ / 0 °C

4.1: 62 percent / EDAC; HOBT; N-ethylmorpholine / CH₂Cl₂ / 1 h / 0 °C

With N-ethylmorpholine;; 2,6-dimethylpyridine; trifluoromethylsulfonic anhydride; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ja003770j

Reference yield:

: 100-51-6,185532-71-2
benzyl alcohol

: 374756-56-6
N-[(2-S-benzyloxycarbonylamino-propanoylamino)methyl] 2-S-methanesulfanyl succinamic acid benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: TFAA / 0 °C

1.2: 86 percent / 20 °C

2.1: 58 percent / K₃CO₃ / dimethylformamide / 96 h / 20 °C

3.1: 2,6-lutidine; triflic anhydride / CH₂Cl₂ / 4 h / -78 °C

3.2: 76 percent / 15-crown-5 / CH₂Cl₂; dimethylformamide / -78 - 20 °C

4.1: 100 percent / TFA / CH₂Cl₂ / 0 °C

5.1: 62 percent / EDAC; HOBT; N-ethylmorpholine / CH₂Cl₂ / 1 h / 0 °C

With N-ethylmorpholine;; 2,6-dimethylpyridine; trifluoromethylsulfonic anhydride; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; trifluoroacetic anhydride; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ja003770j