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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060250Generated: November 2, 2026

5-tert-Butyl-2-(chloromethyl)-1,3-oxazole → N-[5-[[(5-tert-Butyl-2-oxazolyl)methyl]thio]-2-thiazolyl]acetamide

https://huagongshe.com/reaction/1060250

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-tert-Butyl-2-(chloromethyl)-1,3-oxazoleHCID 12968974—
ReactantS-(2-(Acetylamino)-5-thiazolyl) ethanethioateHCID 22481077—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductN-[5-[[(5-tert-Butyl-2-oxazolyl)methyl]thio]-2-thiazolyl]acetamideHCID 532966561%

Reaction Steps

To a solution of 50 mg (0.23 mmol, Applied Chemical Laboratory) of N-[5-(acetylthio)-2-thiazolyl]acetamide in 10 mL of THF was added 0.25 mL of potassium tert-butoxide solution (1 M solution, 0.25 mmol) at rt under argon. The resulting suspension was stirred for 15 min at rt, then a solution of 59 mg of 2-(chloromethyl)-5-t-butyloxazole (0.34 mmol) in 1 mL of THF was added. The resulting mixture was stirred at rt for 16 h, concentrated under reduced pressure and purified by flash column chromatography (silica gel, 25×200 mm, 1:1 EtOAc/hexanes followed by 100% EtOAc) to give 44 mg (0.14 mmol, 61%) of N-[5-[[(5-t-butyl-2-oxazolyl)methyl]thio]-2-thiazolyl]acetamide as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06521759B2
Source datasetuspto-grants-2003_02
ORD IDord-efd2a8d6019848dda5b91fe3ce892e70
Source noteuspto-grants-2003_02