3-cyclopentyl-2-(4-methanesulfonyl-3-nitrophenyl)-N-thiazol-2-yl-propionamide

Base Information

Chemical Name:3-cyclopentyl-2-(4-methanesulfonyl-3-nitrophenyl)-N-thiazol-2-yl-propionamide
CAS No.:300353-14-4
Molecular Formula:C₁₈H₂₁N₃O₅S₂
Molecular Weight:423.514
Hs Code.:

Synonyms:3-cyclopentyl-2-(4-methanesulfonyl-3-nitrophenyl)-N-thiazol-2-yl-propionamide

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Chemical Property of 3-cyclopentyl-2-(4-methanesulfonyl-3-nitrophenyl)-N-thiazol-2-yl-propionamide

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Technology Process of 3-cyclopentyl-2-(4-methanesulfonyl-3-nitrophenyl)-N-thiazol-2-yl-propionamide

There total 2 articles about 3-cyclopentyl-2-(4-methanesulfonyl-3-nitrophenyl)-N-thiazol-2-yl-propionamide 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: 52.0%

: 96-50-4
2-thiazolylamine

: 300355-26-4
3-cyclopentyl-2-(4-methanesulfonyl-3-nitrophenyl)propionic acid

: 300353-14-4
3-cyclopentyl-2-(4-methanesulfonyl-3-nitrophenyl)-N-thiazol-2-yl-propionamide

Guidance literature:: With N-Bromosuccinimide; triphenylphosphine; In dichloromethane;

Reference yield:

: 300355-23-1
4-chloro-3-nitrophenylacetic acid methyl ester

: 300353-14-4
3-cyclopentyl-2-(4-methanesulfonyl-3-nitrophenyl)-N-thiazol-2-yl-propionamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-butyllithium; 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; diisopropylamine / hexane; tetrahydrofuran / 1.15 h / -78 °C / Inert atmosphere

1.2: 48 h / -78 - 25 °C / Inert atmosphere

2.1: dimethyl sulfoxide / 5 h / 130 °C

3.1: lithium hydroxide / water; tetrahydrofuran / 3 h / 25 °C

4.1: triphenylphosphine; N-Bromosuccinimide / dichloromethane / 0.5 h / 0 - 25 °C / Inert atmosphere

4.2: 15 h / 25 °C / Inert atmosphere

With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; N-Bromosuccinimide; n-butyllithium; diisopropylamine; triphenylphosphine; lithium hydroxide; In tetrahydrofuran; hexane; dichloromethane; water; dimethyl sulfoxide;
DOI:10.1021/jm3008689