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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912788Generated: November 3, 2026

1-Chloro-4-isocyanato-2-(trifluoromethyl) benzene → HCID 23155264, compound

https://huagongshe.com/reaction/1912788

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-isocyanato-2-(trifluoromethyl) benzeneHCID 2733265—
ReactantHCID 23155121HCID 23155121—
SolventDichloromethaneHCID 6344—
ProductHCID 23155264HCID 2315526416.4%

Reaction Steps

In 5 mL of methylene chloride, 37 mg of N-(4-imidazo[4,5-c]pyridin-1-yl-phenyl)hydroxylamine obtained in Step A was dissolved, and 41 mg (1.84 mmol) of 4-chloro-3-(trifluoromethyl)phenyl isocyanate was added thereto and the mixture solution was stirred at room temperature for three hours. The reaction solution was concentrated, and then the residue was partitioned between ethyl acetate and a saturated ammonium chloride aqueous solution. The organic layer was washed with a saturated sodium chloride solution, dried and concentrated under reduced pressure. The residue was triturated with n-hexane:ethyl acetate=1:1 to obtain 12 mg (16%) of 1-(4-chloro-3-(trifluoromethyl)phenyl)-3-hydroxy-3-(4-imidazo-[4,5-c]pyridin-1-ylphenyl)urea (Table 1, Compound No. 45) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609656B2
Source datasetuspto-grants-2013_12
ORD IDord-c9971faf3b644b118e3fdc9040130bd5
Source noteuspto-grants-2013_12