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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397309Generated: October 31, 2026

2-[4-(4-Chlorophenyl)-1,3-thiazol-2-yl]ethanamine → N-(2-(4-(4-Chlorophenyl)thiazol-2-yl)ethyl)-3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzamide

https://huagongshe.com/reaction/1397309

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[4-(4-Chlorophenyl)-1,3-thiazol-2-yl]ethanamineHCID 1497769—
Reactant3-(5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acidHCID 25180854—
ProductN-(2-(4-(4-Chlorophenyl)thiazol-2-yl)ethyl)-3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzamideHCID 6737949716%

Reaction Steps

This compound was synthesized from 2-(4-(4-chlorophenyl)thiazol-2-yl)ethanamine and 3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acid as described in example 8 step 6 (30 mg, yield 16%). 1H NMR (400 MHz, CDCl3) δ 8.53 (s, 1H), 8.26 (d, J=7.8 Hz, 1H), 8.06 (d, J=7.8 Hz, 1H), 7.81 (d, J=8.6 Hz, 2H), 7.64-7.60 (m, 2H), 7.39 (s, 1H), 7.34 (d, J=8.6 Hz, 2H), 4.02-3.97 (q, J=5.8 Hz, 2H), 3.39-3.36 (t, J=5.9 Hz, 2H). MS (ESI) m/z: Calculated for C21H14ClF3N4O2S: 478.05. found: 479.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901156B2
Source datasetuspto-grants-2014_12
ORD IDord-9dbc24d085f2476ca59a1e976bbe701d
Source noteuspto-grants-2014_12