(S)-3-amino-2-{[5-(3-hydroxybenzylcarbamoyl)-3-tert-butylthiophene-2-carbonyl]amino}propionic acid methyl ester trifluoroacetic acid salt

Base Information

Chemical Name:(S)-3-amino-2-{[5-(3-hydroxybenzylcarbamoyl)-3-tert-butylthiophene-2-carbonyl]amino}propionic acid methyl ester trifluoroacetic acid salt
CAS No.:1400661-65-5
Molecular Formula:C₂HF₃O₂*C₂₁H₂₇N₃O₅S
Molecular Weight:547.552
Hs Code.:

Synonyms:(S)-3-amino-2-{[5-(3-hydroxybenzylcarbamoyl)-3-tert-butylthiophene-2-carbonyl]amino}propionic acid methyl ester trifluoroacetic acid salt

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Chemical Property of (S)-3-amino-2-{[5-(3-hydroxybenzylcarbamoyl)-3-tert-butylthiophene-2-carbonyl]amino}propionic acid methyl ester trifluoroacetic acid salt

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Technology Process of (S)-3-amino-2-{[5-(3-hydroxybenzylcarbamoyl)-3-tert-butylthiophene-2-carbonyl]amino}propionic acid methyl ester trifluoroacetic acid salt

There total 10 articles about (S)-3-amino-2-{[5-(3-hydroxybenzylcarbamoyl)-3-tert-butylthiophene-2-carbonyl]amino}propionic acid methyl ester trifluoroacetic acid salt 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:

: C₂₆H₃₅N₃O₇S

: 76-05-1
trifluoroacetic acid

: 1400661-65-5
(S)-3-amino-2-{[5-(3-hydroxybenzylcarbamoyl)-3-tert-butylthiophene-2-carbonyl]amino}propionic acid methyl ester trifluoroacetic acid salt

Guidance literature:: In dichloromethane; at 20 ℃; for 0.5h;

Reference yield:

: 873-62-1
m-cyanophenol

: 1400661-65-5
(S)-3-amino-2-{[5-(3-hydroxybenzylcarbamoyl)-3-tert-butylthiophene-2-carbonyl]amino}propionic acid methyl ester trifluoroacetic acid salt

Guidance literature:: Multi-step reaction with 6 steps

1: 1H-imidazole / N,N-dimethyl-formamide / 0 - 20 °C

2: hydrogen / palladium 10% on activated carbon / methanol / 4.5 h / 20 °C / 2585.81 Torr

3: triethylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / N,N-dimethyl-formamide / 0.33 h / 20 °C

4: water; lithium hydroxide monohydrate / tetrahydrofuran / 20 °C

5: triethylamine; dicyclohexyl-carbodiimide / tetrahydrofuran / 20 °C

6: dichloromethane / 0.5 h / 20 °C

With 1H-imidazole; lithium hydroxide monohydrate; water; hydrogen; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; dicyclohexyl-carbodiimide; palladium 10% on activated carbon; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 160833-27-2
3-(tert-butyldimethylsilyloxy)benzonitrile

: 1400661-65-5
(S)-3-amino-2-{[5-(3-hydroxybenzylcarbamoyl)-3-tert-butylthiophene-2-carbonyl]amino}propionic acid methyl ester trifluoroacetic acid salt

Guidance literature:: Multi-step reaction with 5 steps

1: hydrogen / palladium 10% on activated carbon / methanol / 4.5 h / 20 °C / 2585.81 Torr

2: triethylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / N,N-dimethyl-formamide / 0.33 h / 20 °C

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

4: triethylamine; dicyclohexyl-carbodiimide / tetrahydrofuran / 20 °C

5: dichloromethane / 0.5 h / 20 °C

With lithium hydroxide monohydrate; water; hydrogen; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; dicyclohexyl-carbodiimide; palladium 10% on activated carbon; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;