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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803853Generated: November 1, 2026

Water → 3-chloromethyl-N-[5-(3,5-difluoro-benzyloxy)-1H-indazol-3-yl]-benzamide

https://huagongshe.com/reaction/1803853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-(Chloromethyl)benzoyl chlorideHCID 2733324—
Reactant5-[(3,5-difluorobenzyl)oxy]-1H-indazol-3-amineHCID 66997048—
Solvent2,4,6-TrimethylpyridineHCID 7953—
Product3-chloromethyl-N-[5-(3,5-difluoro-benzyloxy)-1H-indazol-3-yl]-benzamideHCID 4624483156%

Reaction Conditions

Temperature4 °C

Reaction Steps

5-(3,5-Difluoro-benzyloxy)-1H-indazol-3-ylamine (550 mg, 2 mmol) was dissolved in sym-collidine, cooled to 4° C. and treated with neat 3-chloromethyl-benzoyl chloride (0.34 mL, 2.4 mmol). After 1 hour the reaction mixture was added drop wise into iced water, with stirring and separation of a yellow oil occurred. Then, EtOAc (50 mL) and 2N HCl (25 mL) were added. The organic phase was separated, washed with aqueous NaHCO3 (50 mL), brine, dried over sodium sulfate and evaporated to dryness. After purification over silica gel (eluent: DCM:MeOH 95:5) 378 mg of title compound were obtained as a whitish solid in 56% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354399B2
Source datasetuspto-grants-2013_01
ORD IDord-f75a9373fc1446e1beb6364fdd07b40d
Source noteuspto-grants-2013_01