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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1685537Generated: November 2, 2026

3-Cyclopentyl-2-(4-methanesulfonyl-phenyl)propionic acid → 3-Cyclopentyl-2-(4-methanesulfonyl-phenyl)-N-[4-methyl-5-(4-methylpiperazine-1-sulfonyl)-thiazol-2-yl]-propionamide

https://huagongshe.com/reaction/1685537

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyclopentyl-2-(4-methanesulfonyl-phenyl)propionic acidHCID 12069489—
Reactant4-Methyl-5-(4-methyl-piperazine-1-sulfonyl)-thiazol-2-ylamineHCID 63946172—
Product3-Cyclopentyl-2-(4-methanesulfonyl-phenyl)-N-[4-methyl-5-(4-methylpiperazine-1-sulfonyl)-thiazol-2-yl]-propionamideHCID 11692512—

Reaction Steps

3-Cyclopentyl-2-(4-methanesulfonyl-phenyl)-N-[4-methyl-5-(4-methylpiperazine-1-sulfonyl)-thiazol-2-yl]-propionamide was prepared from 3-cyclopentyl-2-(4-methanesulfonylphenyl)propionic acid and 4-methyl-5-(4-methyl-piperazine-1-sulfonyl)-thiazol-2-ylamine as described in Example 1. 1H-NMR (CDCl3): δ 13.03 (broad s, 1H), 7.91 (d, 2H), 7.64 (d, 2H), 4.05 (t, 1H), 3.20 (s, 3H), 2.99 (m, 4H), 2.47 (s, 3H), 2.39 (m, 4H), 2.16 (m, 4H), 1.84-1.77 (m, 1H), 1.75-1.39 (m, 7H), 1.19-1.07 (m, 2H); HPLC-MS: m/z=555 (M+1); Rt=3.08 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148412B2
Source datasetuspto-grants-2012_04
ORD IDord-e8bca59ec60a4e0db1909779c9b723a7
Source noteuspto-grants-2012_04