N-[(1S,2R)-2-hydroxy-3-[[(4-methoxyphenyl)sulfonyl][2-methylpropyl]amino]-1-(phenylmethyl)propyl]-4-oxo-2-pentenamide

Base Information

Chemical Name:N-[(1S,2R)-2-hydroxy-3-[[(4-methoxyphenyl)sulfonyl][2-methylpropyl]amino]-1-(phenylmethyl)propyl]-4-oxo-2-pentenamide
CAS No.:918295-04-2
Molecular Formula:C₂₆H₃₄N₂O₆S
Molecular Weight:502.632
Hs Code.:

Synonyms:N-[(1S,2R)-2-hydroxy-3-[[(4-methoxyphenyl)sulfonyl][2-methylpropyl]amino]-1-(phenylmethyl)propyl]-4-oxo-2-pentenamide

Suppliers and Price of N-[(1S,2R)-2-hydroxy-3-[[(4-methoxyphenyl)sulfonyl][2-methylpropyl]amino]-1-(phenylmethyl)propyl]-4-oxo-2-pentenamide

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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 N-[(1S,2R)-2-hydroxy-3-[[(4-methoxyphenyl)sulfonyl][2-methylpropyl]amino]-1-(phenylmethyl)propyl]-4-oxo-2-pentenamide

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Technology Process of N-[(1S,2R)-2-hydroxy-3-[[(4-methoxyphenyl)sulfonyl][2-methylpropyl]amino]-1-(phenylmethyl)propyl]-4-oxo-2-pentenamide

There total 1 articles about N-[(1S,2R)-2-hydroxy-3-[[(4-methoxyphenyl)sulfonyl][2-methylpropyl]amino]-1-(phenylmethyl)propyl]-4-oxo-2-pentenamide 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: 89.0%

: 4743-82-2
4-oxo-2-pentenoic acid

: 159005-71-7
N-((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-N-isobutyl-4-methoxybenzenesulfonamide

: 918295-04-2
N-[(1S,2R)-2-hydroxy-3-[[(4-methoxyphenyl)sulfonyl][2-methylpropyl]amino]-1-(phenylmethyl)propyl]-4-oxo-2-pentenamide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; water; at 0 - 4 ℃;
DOI:10.1021/jm8009525