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(S)-3-<<1-(cyclohexylmethyl)-3,3-difluoro-4-<<2-(4-morpholino)ethyl>amino>-2,4-dioxobutyl>amino>-N--3-oxo-DL-alanine methyl ester methanesulfonate

Base Information
  • Chemical Name:(S)-3-<<1-(cyclohexylmethyl)-3,3-difluoro-4-<<2-(4-morpholino)ethyl>amino>-2,4-dioxobutyl>amino>-N--3-oxo-DL-alanine methyl ester methanesulfonate
  • CAS No.:134334-94-4
  • Molecular Formula:C34H50F2N6O10S
  • Molecular Weight:772.868
  • Hs Code.:
(S)-3-<<1-(cyclohexylmethyl)-3,3-difluoro-4-<<2-(4-morpholino)ethyl>amino>-2,4-dioxobutyl>amino>-N-<N-(4-morpholinosulfonyl)-L-phenylalanyl>-3-oxo-DL-alanine methyl ester methanesulfonate

Synonyms:

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Chemical Property of (S)-3-<<1-(cyclohexylmethyl)-3,3-difluoro-4-<<2-(4-morpholino)ethyl>amino>-2,4-dioxobutyl>amino>-N--3-oxo-DL-alanine methyl ester methanesulfonate
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Technology Process of (S)-3-<<1-(cyclohexylmethyl)-3,3-difluoro-4-<<2-(4-morpholino)ethyl>amino>-2,4-dioxobutyl>amino>-N--3-oxo-DL-alanine methyl ester methanesulfonate

There total 12 articles about (S)-3-<<1-(cyclohexylmethyl)-3,3-difluoro-4-<<2-(4-morpholino)ethyl>amino>-2,4-dioxobutyl>amino>-N--3-oxo-DL-alanine methyl ester methanesulfonate 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:
Guidance literature:
Multi-step reaction with 4 steps
1: 67 percent / dicyclohexylcarbodiimide, HOBT, triethylamine / CH2Cl2; dimethylformamide
2: 97.4 percent / H2 / 20percent Pd/C / methanol / 2 h
3: 34 percent / HOBT, dicyclohexylcarbodiimide / CH2Cl2 / 1.) 0 deg C - RT, overnight, 2.) RT, 38 h
4: 86 percent / 1.) dichloroacetic acid, DMSO, dicyclohexylcarbodiimide, 2.) oxalic acid / 1.) CH2Cl2, a) 0 deg C - RT, overnight, b) RT, 24 h, 2.) CH2Cl2, metanol, 30 min
With dichloro-acetic acid; hydrogen; oxalic acid; benzotriazol-1-ol; dimethyl sulfoxide; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm00111a002
Guidance literature:
Multi-step reaction with 3 steps
1: 97.4 percent / H2 / 20percent Pd/C / methanol / 2 h
2: 34 percent / HOBT, dicyclohexylcarbodiimide / CH2Cl2 / 1.) 0 deg C - RT, overnight, 2.) RT, 38 h
3: 86 percent / 1.) dichloroacetic acid, DMSO, dicyclohexylcarbodiimide, 2.) oxalic acid / 1.) CH2Cl2, a) 0 deg C - RT, overnight, b) RT, 24 h, 2.) CH2Cl2, metanol, 30 min
With dichloro-acetic acid; hydrogen; oxalic acid; benzotriazol-1-ol; dimethyl sulfoxide; dicyclohexyl-carbodiimide; palladium on activated charcoal; In methanol; dichloromethane;
DOI:10.1021/jm00111a002
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