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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892623Generated: October 30, 2026

Chloroacetyl chloride → HCID 131716539, compound

https://huagongshe.com/reaction/892623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantTetrahydrofuranHCID 8028—
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 9991469HCID 9991469—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 131716539HCID 13171653956%

Reaction Steps

Chloroacetyl chloride (2.2 g) was added dropwise to a mixture of 2-phenyl-5,6,7,8-tetrahydro-4H-thiazolo[5,4-b]azepine (3.0 g), triethylamine (3.6 ml) and methylenechloride (100 ml) under ice-cooling and stirring. After stirring for 30 mins. at room temperature, the mixture was distilled under reduced pressure to remove the solvent, and the residue was extracted with chloroform. The extract was washed with a saturated sodium hydrogen carbonate solution, water, dried over anhydrous sodium sulfate and the solvent removed by distillation under reduced pressure to give a crude product (4.0 g). To a solution of the above product (1.9 g) and triethylamine (2.6 ml) in 20 ml of THF was added N-methylpiperazine (1.4 ml), and the whole was stirred for 5 hrs. at room temperature. The reaction mixture was concentrated and extracted with ethyl ether. The extract was washed with water, dried and concentrated under reduced pressure. The residue was purified by a column chromatography on silica gel, converted into a salt of hydrochloric acid and then recrystallized from a mixture of isopropanol and ethyl ether to give the title compound (1.66 g, 56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05118806
Source datasetuspto-grants-1992_06
ORD IDord-1fe80b4cdd9e42bc8dbd8698cc92831c
Source noteuspto-grants-1992_06