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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582142Generated: October 26, 2026

4-Fluorobenzoyl chloride → N-(7-cyclohexyl-4-methoxy-benzothiazol-2-yl)-4-fluoro-benzamide

https://huagongshe.com/reaction/1582142

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzoyl chlorideHCID 67879—
ReactantDiisopropylethylamineHCID 81531—
Reactant7-Cyclohexyl-4-methoxy-benzothiazol-2-ylamineHCID 22719574—
SolventTetrahydrofuranHCID 8028—
ProductN-(7-cyclohexyl-4-methoxy-benzothiazol-2-yl)-4-fluoro-benzamideHCID 995203414%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 0.05 g (0.19 mMol) 7-cyclohexyl-4-methoxy-benzothiazol-2-ylamine in 2 ml THF were added 0.1 ml ethyl diisopropyl amine and 0.027 ml (0.23 mMol) 4-fluoro-benzoyl chloride. The reaction mixture was heated to 70° C. for 2 h. The solvent was evaporated to dryness, the residue taken up in dichloro methane and washed with water and brine. The organic phase was dried over sodium sulfate and evaporated to dryness in vacuo. The residue was subjected to column chromatography (ethyl acetate/hexane 1:9, 1:4) to yield 0.01 g (14%) of N-(7-cyclohexyl-4-methoxy-benzothiazol-2-yl)-4-fluoro-benzamide as a light yellow solid; F.p.: 192-195° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734179B2
Source datasetuspto-grants-2004_05
ORD IDord-d6d6fc2e4af94ca5b8ce9d321944528c
Source noteuspto-grants-2004_05