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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587408Generated: November 3, 2026

Dichloromethane → HCID 19757951, compound

https://huagongshe.com/reaction/1587408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 19757968HCID 19757968—
ProductHCID 19757951HCID 19757951—

Reaction Steps

A mixture of 4,5-bis(4methyoxyphenyl)-2-piperazin-1-ylcarbonylthiazole hydrochloride (0.40 g) in dichloromethane (30 ml) was added to a saturated aqueous solution of sodium hydrogencarbonate, and extracted with dichloromethane. The separated organic layer was washed with brine and dried over magnesium sulfate. After filtration, the filtrate was evaporated in vacuo. The resulting residue was dissolved in a mixture of dichloromethane (10 ml) and triethylamine (0.14 ml). To the mixture was added dropwise a solution of acetyl chloride (0.07 ml) in dichloromethane (5 ml), at 0° to 5° C., and the reaction mixture was stirred at ambient temperature for 30 minutes. The resulting mixture was poured into water, and adjusted to pH 11 with aqueous solution of potassium carbonate, and extracted with dichloromethane. The separated organic layer was washed with a saturated aqueous solution of sodium hydrogencarbonate, water, dilute hydrochloric acid, water, and brine, and dried over magnesium sulfate and treated with activated charcoal. After filtration, the filtrate was evaporated in vacuo. The resulting residue was recrystallized from a mixture of isopropyl ether and ethanol to give a crystal of 2-(4acetylpiperazin-1-yl)carbonyl-4,5-bis(4methoxyphenyl)thiazole (0.18 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05217971
Source datasetuspto-grants-1993_06
ORD IDord-5ee41521f599458ba11efe38e2ba7379
Source noteuspto-grants-1993_06