(3S,4RS)-4-hydroxy-3-<-L-prolyl>amino>-5-phenoxypentanoic acid tert-butyl ester

Base Information

Chemical Name:(3S,4RS)-4-hydroxy-3-<-L-prolyl>amino>-5-phenoxypentanoic acid tert-butyl ester
CAS No.:221106-14-5
Molecular Formula:C₃₁H₄₈N₄O₈
Molecular Weight:604.744
Hs Code.:

(3S,4RS)-4-hydroxy-3-<<N-<N-(1-morpholinomethylcarbonyl)-L-valyl>-L-prolyl>amino>-5-phenoxypentanoic acid tert-butyl ester

Synonyms:(3S,4RS)-4-hydroxy-3-<-L-prolyl>amino>-5-phenoxypentanoic acid tert-butyl ester

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (3S,4RS)-4-hydroxy-3-<-L-prolyl>amino>-5-phenoxypentanoic acid tert-butyl ester

Chemical Property:

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Technology Process of (3S,4RS)-4-hydroxy-3-<-L-prolyl>amino>-5-phenoxypentanoic acid tert-butyl ester

There total 5 articles about (3S,4RS)-4-hydroxy-3-<-L-prolyl>amino>-5-phenoxypentanoic acid tert-butyl 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: 100.0%

: 110-91-8,99108-56-2
morpholine

: 221106-12-3
(3S,4RS)-3-<amino>-4-hydroxy-5-phenoxypentanoic acid tert-butyl ester

: 221106-14-5
(3S,4RS)-4-hydroxy-3-<-L-prolyl>amino>-5-phenoxypentanoic acid tert-butyl ester

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1248/cpb.47.11

Reference yield:

: 47450-18-0,68166-40-5,53331-43-4
N-benzyloxycarbonyl-L-valyl-L-proline

: 221106-14-5
(3S,4RS)-4-hydroxy-3-<-L-prolyl>amino>-5-phenoxypentanoic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 77 percent / 1-hydroxybenzotriazole, N-methylmorpholine, 1-ethyl-3-dimethylaminopropylcarbodiimide monohydrochloride / CH₂Cl₂ / 12 h / Ambient temperature

2: 98 percent / H₂ / 10 percent Pd/C / methanol / Ambient temperature

3: 88 percent / triethylamine / CH₂Cl₂ / 1 h

4: 100 percent / diisopropylethylamine / CH₂Cl₂

With 4-methyl-morpholine; hydrogen; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In methanol; dichloromethane;
DOI:10.1248/cpb.47.11

Reference yield:

: 221106-03-2
(3S,4RS)-3-amino-4-hydroxy-5-phenoxypentanoic acid tert-butyl ester

: 221106-14-5
(3S,4RS)-4-hydroxy-3-<-L-prolyl>amino>-5-phenoxypentanoic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 77 percent / 1-hydroxybenzotriazole, N-methylmorpholine, 1-ethyl-3-dimethylaminopropylcarbodiimide monohydrochloride / CH₂Cl₂ / 12 h / Ambient temperature

2: 98 percent / H₂ / 10 percent Pd/C / methanol / Ambient temperature

3: 88 percent / triethylamine / CH₂Cl₂ / 1 h

4: 100 percent / diisopropylethylamine / CH₂Cl₂

With 4-methyl-morpholine; hydrogen; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In methanol; dichloromethane;
DOI:10.1248/cpb.47.11