(2S,4S,5S,7S)-5-amino-N-(2,2-dimethyl-3-(4-methylphenylsulfonamido)propyl)-4-hydroxy-2-isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-8-methylnonanamide

Base Information

Chemical Name:(2S,4S,5S,7S)-5-amino-N-(2,2-dimethyl-3-(4-methylphenylsulfonamido)propyl)-4-hydroxy-2-isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-8-methylnonanamide
CAS No.:1321622-27-8
Molecular Formula:C₃₇H₆₁N₃O₇S
Molecular Weight:691.973
Hs Code.:

(2S,4S,5S,7S)-5-amino-N-(2,2-dimethyl-3-(4-methylphenylsulfonamido)propyl)-4-hydroxy-2-isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-8-methylnonanamide

Synonyms:(2S,4S,5S,7S)-5-amino-N-(2,2-dimethyl-3-(4-methylphenylsulfonamido)propyl)-4-hydroxy-2-isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-8-methylnonanamide

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Chemical Property of (2S,4S,5S,7S)-5-amino-N-(2,2-dimethyl-3-(4-methylphenylsulfonamido)propyl)-4-hydroxy-2-isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-8-methylnonanamide

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Technology Process of (2S,4S,5S,7S)-5-amino-N-(2,2-dimethyl-3-(4-methylphenylsulfonamido)propyl)-4-hydroxy-2-isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-8-methylnonanamide

There total 8 articles about (2S,4S,5S,7S)-5-amino-N-(2,2-dimethyl-3-(4-methylphenylsulfonamido)propyl)-4-hydroxy-2-isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-8-methylnonanamide 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: 93.8%

: 1321622-45-0
(2S,4S,5S,7S)-5-azido-N-(2,2-dimethyl-3-(4-methylphenylsulfonamido)propyl)-4-hydroxy-2-isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-8-methylnonanamide

: 1321622-27-8
(2S,4S,5S,7S)-5-amino-N-(2,2-dimethyl-3-(4-methylphenylsulfonamido)propyl)-4-hydroxy-2-isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-8-methylnonanamide

Guidance literature:: With palladium 10% on activated carbon; hydrogen; ethanolamine; In tert-butyl methyl ether; at 25 ℃;
DOI:10.1016/j.bmc.2011.05.059

Reference yield:

: 1321622-63-2
N-(3-amino-2,2-dimethylpropyl)-4-methylbenzenesulfon-amide

: 1321622-27-8
(2S,4S,5S,7S)-5-amino-N-(2,2-dimethyl-3-(4-methylphenylsulfonamido)propyl)-4-hydroxy-2-isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-8-methylnonanamide

Guidance literature:: Multi-step reaction with 2 steps

1: 2-hydroxypyridin; triethylamine / 65 °C

2: palladium 10% on activated carbon; hydrogen; ethanolamine / tert-butyl methyl ether / 25 °C

With 2-hydroxypyridin; palladium 10% on activated carbon; hydrogen; ethanolamine; triethylamine; In tert-butyl methyl ether;
DOI:10.1016/j.bmc.2011.05.059

Reference yield:

: 1321622-79-0
N-(3-azido-2,2-dimethylpropyl)-4-methylbenzenesulfonamide

: 1321622-27-8
(2S,4S,5S,7S)-5-amino-N-(2,2-dimethyl-3-(4-methylphenylsulfonamido)propyl)-4-hydroxy-2-isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-8-methylnonanamide

Guidance literature:: Multi-step reaction with 3 steps

1: palladium 10% on activated carbon; hydrogen / methanol / 25 °C

2: 2-hydroxypyridin; triethylamine / 65 °C

3: palladium 10% on activated carbon; hydrogen; ethanolamine / tert-butyl methyl ether / 25 °C

With 2-hydroxypyridin; palladium 10% on activated carbon; hydrogen; ethanolamine; triethylamine; In methanol; tert-butyl methyl ether;
DOI:10.1016/j.bmc.2011.05.059