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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420593Generated: October 26, 2026

Dimethylformamide → [3-[[[1-(6-Chlorobenzothiazole-2-yl)piperidine-4-yl]isopropylamino]methyl]phenyl]acetic acid methyl ester

https://huagongshe.com/reaction/420593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant(3-Bromomethyl-phenyl)-acetic acid methyl esterHCID 10014651—
ReactantHCID 57966227HCID 57966227—
SolventWaterHCID 962—
Product[3-[[[1-(6-Chlorobenzothiazole-2-yl)piperidine-4-yl]isopropylamino]methyl]phenyl]acetic acid methyl esterHCID 5796626137.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of [1-(6-chlorobenzothiazole-2-yl)piperidine-4-yl]isopropylamine (159 mg), (3-bromomethylphenyl)acetic acid methyl ester (138 mg), potassium carbonate (107 mg) and dimethylformamide (2 mL) was stirred at 80° C. for 8 hours. To the reaction solution was added water and extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over magnesium sulphate. The solvent was evaporated under reduced pressure and the residue was purified by column chromatograph on silica gel to give the title compound (90 mg). Yield: 37%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097610B2
Source datasetuspto-grants-2012_01
ORD IDord-01c0932a77704c018ac6565d88b64913
Source noteuspto-grants-2012_01