(2R,3S,4R)-2-amino-4-(N-(((tert)-butyloxy)carbonyl)-amino)-3-hydroxy-5-(1-naphthyl)-1-phenylpentane acetonide

Base Information

Chemical Name:(2R,3S,4R)-2-amino-4-(N-(((tert)-butyloxy)carbonyl)-amino)-3-hydroxy-5-(1-naphthyl)-1-phenylpentane acetonide
CAS No.:148472-72-4
Molecular Formula:C₂₉H₃₆N₂O₃
Molecular Weight:460.616
Hs Code.:

Synonyms:(2R,3S,4R)-2-amino-4-(N-(((tert)-butyloxy)carbonyl)-amino)-3-hydroxy-5-(1-naphthyl)-1-phenylpentane acetonide

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Chemical Property of (2R,3S,4R)-2-amino-4-(N-(((tert)-butyloxy)carbonyl)-amino)-3-hydroxy-5-(1-naphthyl)-1-phenylpentane acetonide

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Technology Process of (2R,3S,4R)-2-amino-4-(N-(((tert)-butyloxy)carbonyl)-amino)-3-hydroxy-5-(1-naphthyl)-1-phenylpentane acetonide

There total 5 articles about (2R,3S,4R)-2-amino-4-(N-(((tert)-butyloxy)carbonyl)-amino)-3-hydroxy-5-(1-naphthyl)-1-phenylpentane acetonide 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: 46.0%

: 148472-69-9
(2R,3S,4R)-4-(N-(((tert)-butyloxy)carbonyl)-amino)-2-(N-((benzyloxy)carbonyl)-amino)-3-hydroxy-5-(1-naphthyl)-1-phenylpentane acetonide

: 148472-72-4
(2R,3S,4R)-2-amino-4-(N-(((tert)-butyloxy)carbonyl)-amino)-3-hydroxy-5-(1-naphthyl)-1-phenylpentane acetonide

Guidance literature:: With hydrogen; palladium on activated charcoal; In acetic acid; for 21h;
DOI:10.1016/S0040-4020(01)80342-2

Reference yield:

: (S)-2-Naphthalen-1-ylmethyl-3,5-dioxo-pyrrolidine-1-carboxylic acid tert-butyl ester

: 148472-72-4
(2R,3S,4R)-2-amino-4-(N-(((tert)-butyloxy)carbonyl)-amino)-3-hydroxy-5-(1-naphthyl)-1-phenylpentane acetonide

Guidance literature:: Multi-step reaction with 6 steps

1: sodium borohydride / CH₂Cl₂; acetic acid / 3 h

2: 1) HMPA, 2) C₆H₅CH₂Br / 1) THF, -78 degC, 50 min, 2) THF, -78 degC, 30 min

3: 1) 1M LiOH, 2) PPTS / 1) THF, 1.5 h, 2) CH₂Cl₂, r.t., 2 h

4: diphenylphosphoryl azide, Et₃N / xylene / 2 h / 90 °C

5: DMAP / 15 h

6: 46 percent / H₂ / 10percent Pd/C / acetic acid / 21 h

With N,N,N,N,N,N-hexamethylphosphoric triamide; dmap; lithium hydroxide; sodium tetrahydroborate; diphenylphosphoranyl azide; hydrogen; pyridinium p-toluenesulfonate; benzyl bromide; triethylamine; palladium on activated charcoal; In dichloromethane; acetic acid; xylene;
DOI:10.1016/S0040-4020(01)80342-2

Reference yield:

: 148554-94-3
(3R,4S,5R)-N-(((tert)-butyloxy)carbonyl)-3-benzyl-4-hydroxy-5-(1-naphthylmethyl)-2-pyrrolidinone

: 148472-72-4
(2R,3S,4R)-2-amino-4-(N-(((tert)-butyloxy)carbonyl)-amino)-3-hydroxy-5-(1-naphthyl)-1-phenylpentane acetonide

Guidance literature:: Multi-step reaction with 4 steps

1: 1) 1M LiOH, 2) PPTS / 1) THF, 1.5 h, 2) CH₂Cl₂, r.t., 2 h

2: diphenylphosphoryl azide, Et₃N / xylene / 2 h / 90 °C

3: DMAP / 15 h

4: 46 percent / H₂ / 10percent Pd/C / acetic acid / 21 h

With dmap; lithium hydroxide; diphenylphosphoranyl azide; hydrogen; pyridinium p-toluenesulfonate; triethylamine; palladium on activated charcoal; In acetic acid; xylene;
DOI:10.1016/S0040-4020(01)80342-2