(S)-2-{[5-(3-Hydroxy-benzylcarbamoyl)-3-isopropyl-thiophene-2-carbonyl]-amino}-3-[(thiophene-2-carbonyl)-amino]-propionic acid

Base Information

Chemical Name:(S)-2-{[5-(3-Hydroxy-benzylcarbamoyl)-3-isopropyl-thiophene-2-carbonyl]-amino}-3-[(thiophene-2-carbonyl)-amino]-propionic acid
CAS No.:1400660-97-0
Molecular Formula:C₂₄H₂₅N₃O₆S₂
Molecular Weight:515.611
Hs Code.:

Synonyms:(S)-2-{[5-(3-Hydroxy-benzylcarbamoyl)-3-isopropyl-thiophene-2-carbonyl]-amino}-3-[(thiophene-2-carbonyl)-amino]-propionic acid

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Chemical Property of (S)-2-{[5-(3-Hydroxy-benzylcarbamoyl)-3-isopropyl-thiophene-2-carbonyl]-amino}-3-[(thiophene-2-carbonyl)-amino]-propionic acid

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Technology Process of (S)-2-{[5-(3-Hydroxy-benzylcarbamoyl)-3-isopropyl-thiophene-2-carbonyl]-amino}-3-[(thiophene-2-carbonyl)-amino]-propionic acid

There total 8 articles about (S)-2-{[5-(3-Hydroxy-benzylcarbamoyl)-3-isopropyl-thiophene-2-carbonyl]-amino}-3-[(thiophene-2-carbonyl)-amino]-propionic acid 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: 75.0%

: 1400662-38-5
(S)-2-{[5-(3-Hydroxy-benzylcarbamoyl)-3-isopropyl-thiophene-2-carbonyl]-amino}-3-[(thiophene-2-carbonyl)-amino]-propionic acid methyl ester

: 1400660-97-0
(S)-2-{[5-(3-Hydroxy-benzylcarbamoyl)-3-isopropyl-thiophene-2-carbonyl]-amino}-3-[(thiophene-2-carbonyl)-amino]-propionic acid

Guidance literature:: (S)-2-{[5-(3-Hydroxy-benzylcarbamoyl)-3-isopropyl-thiophene-2-carbonyl]-amino}-3-[(thiophene-2-carbonyl)-amino]-propionic acid methyl ester; With lithium hydroxide monohydrate; water; In tetrahydrofuran; at 20 ℃; for 15h;

With hydrogenchloride; In tetrahydrofuran; water;

Reference yield:

: 1400662-35-2
(S)-3-tert-Butoxycarbonylamino-2-{[5-(3-hydroxy-benzylcarbamoyl)-3-isopropyl-thiophene-2-carbonyl]-amino}-propionic acid methyl ester

: 1400660-97-0
(S)-2-{[5-(3-Hydroxy-benzylcarbamoyl)-3-isopropyl-thiophene-2-carbonyl]-amino}-3-[(thiophene-2-carbonyl)-amino]-propionic acid

Guidance literature:: Multi-step reaction with 3 steps

1: dichloromethane / 1 h / 20 °C

2: triethylamine; benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / N,N-dimethyl-formamide / 1.5 h / 20 °C

3: water; lithium hydroxide monohydrate / tetrahydrofuran / 15 h / 20 °C

With lithium hydroxide monohydrate; water; benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1400662-37-4
(S)-3-Amino-2-{[5-(3-hydroxy-benzylcarbamoyl)-3-isopropyl-thiophene-2-carbonyl]-amino}-propionic acid methyl ester trifluoro-acetic acid salt

: 1400660-97-0
(S)-2-{[5-(3-Hydroxy-benzylcarbamoyl)-3-isopropyl-thiophene-2-carbonyl]-amino}-3-[(thiophene-2-carbonyl)-amino]-propionic acid

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine; benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / N,N-dimethyl-formamide / 1.5 h / 20 °C

2: water; lithium hydroxide monohydrate / tetrahydrofuran / 15 h / 20 °C

With lithium hydroxide monohydrate; water; benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; In tetrahydrofuran; N,N-dimethyl-formamide;