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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735142Generated: October 26, 2026

Chloroacetyl chloride → 2-chloro-N-(3-methyl-5,6,7,8-tetrahydrothieno[2,3-b]quinolin-4-yl)acetamid

https://huagongshe.com/reaction/1735142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
Reactant4-Amino-3-methyl-5,6,7,8-tetrahydrothieno[2,3-b]quinolineHCID 15225118—
Product2-chloro-N-(3-methyl-5,6,7,8-tetrahydrothieno[2,3-b]quinolin-4-yl)acetamidHCID 53850020—

Reaction Conditions

Temperature25 °C

Reaction Steps

To 12.7 g of 4-amino-3-methyl-5,6,7,8-tetrahydrothieno[2,3-b]quinoline, was added 40 ml of chloroacetyl chloride, and the mixture was refluxed for 40 minutes. The oil bath was removed and the reaction mixture was added with 50 ml of 1,2-dichloroethane and cooled to 25° C. The precipitated crystals were collected by filtration and washed with 1,2-dichloroethane. The crystals were suspended in a mixed solvent of 250 ml of chloroform, 55 ml of water and 60 ml of ethanol, and 4.3 ml of concentrated ammonia water was added thereto. The suspension was heated to 40° C. to dissolve substantially all the crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536728
Source datasetuspto-grants-1996_07
ORD IDord-f98c14595cbf4cf8a2dfe6118e0c8ab6
Source noteuspto-grants-1996_07