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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582111Generated: November 3, 2026

4-(Chloromethyl)benzoyl chloride → HCID 22719566, compound

https://huagongshe.com/reaction/1582111

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Chloromethyl)benzoyl chlorideHCID 70136—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Methoxy-7-(tetrahydro-pyran-4-yl)-benzothiazol-2-yl-amineHCID 22015735—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22719566HCID 2271956671%

Reaction Steps

To a stirred solution of 250 mg (0.95 mmol) 4-methoxy-7-(tetrahydro-pyran-4-yl)-benzothiazol-2-ylamine and 0.95 ml (5.53 mmol) N-ethyldiisopropylamine in 10 ml THF at room temperature was added dropwise a solution of 216 mg (1.14 mmol) 4-(chloromethyl)benzoyl chloride in 3 ml dichloromethane and stirring continued at room temperature for 60 h. The reaction mixture was then concentrated in vacuo. Flash chromatography (1/1 ethyl acetate/hexane) followed by trituration in ether afforded 280 mg (71%) 4-chloromethyl-N-[4-methoxy-7-(tetrahydro-pyran-4-yl)-benzothiazol-2-yl]-benzamide as a white crystalline solid. ES-MS m/e (%): 441 (M{37Cl}+Na+, 7), 439 (M{35Cl}+Na+, 21). 419 (M{37Cl}+H+, 41), 417 (M{35Cl}+H+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734179B2
Source datasetuspto-grants-2004_05
ORD IDord-89655537c0ef4b4bb327f579c197dd65
Source noteuspto-grants-2004_05