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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637238Generated: November 1, 2026

Benzoyl chloride → N-[5-[[(5-ethyl-2-oxazolyl)methyl]thio]-2-thiazolyl]benzamide

https://huagongshe.com/reaction/1637238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant2-Amino-5-[[(5-ethyl-2-oxazolyl)methyl]thio]-thiazoleHCID 18667982—
SolventDichloromethaneHCID 6344—
ProductN-[5-[[(5-ethyl-2-oxazolyl)methyl]thio]-2-thiazolyl]benzamideHCID 990619059.3%

Reaction Steps

A mixture of 2-amino-5-[[(5-ethyl-2-oxazolyl)methyl]thio]-thiazole (48.2 mg, 0.2 mmol), benzoyl chloride (24.4 mg, 0.21 mmol) and triethylamine (35 mg, 0.35 mmol) in methylene chloride (0.5 mL) was stirred at rt for 10 min. The organic solution was washed with water and concentrated. The residue was purified by a flash column (SiO2 ; hexanes: ethyl acetate/2:1) to afford N-[5-[[(5-ethyl-2-oxazolyl)methyl]thio]-2-thiazolyl]benzamide (41 mg, 59%) as a solid, mp 122-123° C. 1H NMR (CDCl3) δ12.65 (s, 1 H), 7.96 (m, 2 H), 7.61 (m,, 1 H), 7.49 (m, 2 H), 6.88 (s, 1 H), 6.56 (s, 1 H), 3.93 (s, 2 H), 2.61 (q, J=7.6 Hz, 2 H), 1.20 (t, J=7.6 Hz, 3 H); MS m/e 346 (M+H)+ ;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06040321
Source datasetuspto-grants-2000_03
ORD IDord-32e2c3bea13f4b82892149a20741cd1b
Source noteuspto-grants-2000_03