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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644763Generated: October 27, 2026

Triethylamine → 4-{[4-(Methylthio)-1,3-thiazol-2-yl]carbamoyl}phenyl acetate

https://huagongshe.com/reaction/1644763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactantp-Acetoxybenzoyl chlorideHCID 2756254—
Reactant4-(Methylthio)-1,3-thiazol-2-amineHCID 55285798—
SolventTetrahydrofuranHCID 8028—
Product4-{[4-(Methylthio)-1,3-thiazol-2-yl]carbamoyl}phenyl acetateHCID 57571887109%

Reaction Steps

Into a solution of 510 (0.815 g, 4.10 mmol) and dry THF (20.0 mL) was added a solution of triethylamine (0.572 mL, 4.10 mmol) and dry THF (5.00 mL), followed by a solution of 508 (0.500 g, 3.42 mmol) dissolved in dry THF (15.0 mL). The reaction was stirred at room temperature. After stirring overnight, the reaction was concentrated in vacuo. The residue was partitioned between a saturated aqueous sodium bicarbonate and dichloromethane. The dichloromethane layer was washed a second time with the saturated sodium bicarbonate solution and than twice with aq. 1 M HCl. The dichloromethane layer was dried over anhydrous magnesium sulfate and concentrated in vacuo to give crude 82 (1.15 g,>100%) as a brown solid. The crude product was suspended in diethyl ether, stirred and filtered. The filter pad was washed with ether several times, and dried in vacuo to give 82 (0.692 g, 63%) as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124632B2
Source datasetuspto-grants-2012_02
ORD IDord-b2ca73b854d247e69c449ab5d7b9d04f
Source noteuspto-grants-2012_02