(S)-4-(6-Acetoxy-hexylcarbamoyl)-4-((R)-2-benzyloxycarbonylamino-propionylamino)-butyric acid methyl ester

Base Information

Chemical Name:(S)-4-(6-Acetoxy-hexylcarbamoyl)-4-((R)-2-benzyloxycarbonylamino-propionylamino)-butyric acid methyl ester
CAS No.:205252-96-6
Molecular Formula:C₂₅H₃₇N₃O₈
Molecular Weight:507.584
Hs Code.:

Synonyms:(S)-4-(6-Acetoxy-hexylcarbamoyl)-4-((R)-2-benzyloxycarbonylamino-propionylamino)-butyric acid methyl ester

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Chemical Property of (S)-4-(6-Acetoxy-hexylcarbamoyl)-4-((R)-2-benzyloxycarbonylamino-propionylamino)-butyric acid methyl ester

Chemical Property:

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Technology Process of (S)-4-(6-Acetoxy-hexylcarbamoyl)-4-((R)-2-benzyloxycarbonylamino-propionylamino)-butyric acid methyl ester

There total 5 articles about (S)-4-(6-Acetoxy-hexylcarbamoyl)-4-((R)-2-benzyloxycarbonylamino-propionylamino)-butyric 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:

: 4048-33-3
6-amino-1-hexanol

: 205252-96-6
(S)-4-(6-Acetoxy-hexylcarbamoyl)-4-((R)-2-benzyloxycarbonylamino-propionylamino)-butyric acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 87 percent / 2-ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline / CHCl₃ / Ambient temperature

2: 437 mg / 1-hydroxybenzotriazole, 1,3-dicyclohexylcarbodiimide / CH₂Cl₂ / 0 - 20 °C

3: H₂ / 10percent Pd/C / ethanol / 760 Torr / Ambient temperature

4: 1-hydroxybenzotriazole, 1,3-dicyclohexylcarbodiimide / 0 - 20 °C

With hydrogen; benzotriazol-1-ol; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; dicyclohexyl-carbodiimide; palladium on activated charcoal; In ethanol; dichloromethane; chloroform;
DOI:10.1021/jm970734v

Reference yield:

: 4652-65-7
(S)-2-Benzyloxycarbonylamino-pentanedioic acid 5-methyl ester

: 205252-96-6
(S)-4-(6-Acetoxy-hexylcarbamoyl)-4-((R)-2-benzyloxycarbonylamino-propionylamino)-butyric acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 87 percent / 2-ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline / CHCl₃ / Ambient temperature

2: 437 mg / 1-hydroxybenzotriazole, 1,3-dicyclohexylcarbodiimide / CH₂Cl₂ / 0 - 20 °C

3: H₂ / 10percent Pd/C / ethanol / 760 Torr / Ambient temperature

4: 1-hydroxybenzotriazole, 1,3-dicyclohexylcarbodiimide / 0 - 20 °C

With hydrogen; benzotriazol-1-ol; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; dicyclohexyl-carbodiimide; palladium on activated charcoal; In ethanol; dichloromethane; chloroform;
DOI:10.1021/jm970734v

Reference yield:

: 205252-10-4
(S)-4-Benzyloxycarbonylamino-4-(6-hydroxy-hexylcarbamoyl)-butyric acid methyl ester

: 205252-96-6
(S)-4-(6-Acetoxy-hexylcarbamoyl)-4-((R)-2-benzyloxycarbonylamino-propionylamino)-butyric acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 437 mg / 1-hydroxybenzotriazole, 1,3-dicyclohexylcarbodiimide / CH₂Cl₂ / 0 - 20 °C

2: H₂ / 10percent Pd/C / ethanol / 760 Torr / Ambient temperature

3: 1-hydroxybenzotriazole, 1,3-dicyclohexylcarbodiimide / 0 - 20 °C

With hydrogen; benzotriazol-1-ol; dicyclohexyl-carbodiimide; palladium on activated charcoal; In ethanol; dichloromethane;
DOI:10.1021/jm970734v