(2R,5S,6S)-3-aza-2-benzyl-6-[(tert-butyloxycarbonyl)amino]-5-hydroxy-7-phenylheptanoyl amide

Base Information

Chemical Name:(2R,5S,6S)-3-aza-2-benzyl-6-[(tert-butyloxycarbonyl)amino]-5-hydroxy-7-phenylheptanoyl amide
CAS No.:500767-16-8
Molecular Formula:C₂₄H₃₃N₃O₄
Molecular Weight:427.544
Hs Code.:

Synonyms:(2R,5S,6S)-3-aza-2-benzyl-6-[(tert-butyloxycarbonyl)amino]-5-hydroxy-7-phenylheptanoyl amide

Suppliers and Price of (2R,5S,6S)-3-aza-2-benzyl-6-[(tert-butyloxycarbonyl)amino]-5-hydroxy-7-phenylheptanoyl amide

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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 (2R,5S,6S)-3-aza-2-benzyl-6-[(tert-butyloxycarbonyl)amino]-5-hydroxy-7-phenylheptanoyl amide

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Technology Process of (2R,5S,6S)-3-aza-2-benzyl-6-[(tert-butyloxycarbonyl)amino]-5-hydroxy-7-phenylheptanoyl amide

There total 1 articles about (2R,5S,6S)-3-aza-2-benzyl-6-[(tert-butyloxycarbonyl)amino]-5-hydroxy-7-phenylheptanoyl amide 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: 54.0%

: 5241-58-7,5241-59-8,17193-31-6,60058-39-1
D-Phenylalaninamide

: 98760-08-8
(2R,3S)-3-[N-(tert-butyloxycarbonyl)amino]-1,2-epoxy-4-phenylbutane

: 500767-16-8
(2R,5S,6S)-3-aza-2-benzyl-6-[(tert-butyloxycarbonyl)amino]-5-hydroxy-7-phenylheptanoyl amide

Guidance literature:: In isopropyl alcohol; Heating;
DOI:10.1021/jm020951i

Reference yield: 73.0%

: 501-53-1,94274-21-2
benzyl chloroformate

: 500767-16-8
(2R,5S,6S)-3-aza-2-benzyl-6-[(tert-butyloxycarbonyl)amino]-5-hydroxy-7-phenylheptanoyl amide

: 500767-23-7
(2R,5S,6S)-3-aza-2-benzyl-3-(benzyloxycarbonyl)-6-[(tert-butyloxycarbonyl)amino]-5-hydroxy-7-phenylheptanoyl amide

Guidance literature:: With sodium carbonate; In tetrahydrofuran; at 20 ℃;
DOI:10.1021/jm020951i

Reference yield:

: 500767-16-8
(2R,5S,6S)-3-aza-2-benzyl-6-[(tert-butyloxycarbonyl)amino]-5-hydroxy-7-phenylheptanoyl amide

: ((R)-1-Carbamoyl-2-phenyl-ethyl)-((2S,3S)-2-hydroxy-3-{(S)-3-methyl-2-[(pyridine-2-carbonyl)-amino]-butyrylamino}-4-phenyl-butyl)-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 73 percent / aq. Na₂CO₃ / tetrahydrofuran / 20 °C

2: HCl / ethyl acetate / 20 °C

3: 0.43 g / TBTU; DIEA / dimethylformamide / 20 °C

4: HCl / ethyl acetate / 20 °C

5: TBTU; DIEA / dimethylformamide; CH₂Cl₂ / 20 °C

With hydrogenchloride; sodium carbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm020951i