Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366782Generated: November 4, 2026

1-Chloro-4-isocyanato-2-(trifluoromethyl) benzene → N-{5-[4-chloro-3-({[4-chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)phenoxy][1,3]thiazolo[5,4-b]pyridin-2-yl}cyclopropanecarboxamide

https://huagongshe.com/reaction/2366782

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-isocyanato-2-(trifluoromethyl) benzeneHCID 2733265—
ReactantN-[5-(3-amino-4-chlorophenoxy) [1,3]thiazolo[5,4-b]pyridin-2-yl]cyclopropanecarboxamideHCID 57384284—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-{5-[4-chloro-3-({[4-chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)phenoxy][1,3]thiazolo[5,4-b]pyridin-2-yl}cyclopropanecarboxamideHCID 5845128533%

Reaction Steps

N-[5-(3-Amino-4-chlorophenoxy)[1,3]thiazolo[5,4-b]pyridin-2-yl]cyclopropanecarboxamide (120 mg, 0.33 mmol) was dissolved in N,N-dimethylformamide (2.0 ml), 1-chloro-4-isocyanato-2-(trifluoromethyl)benzene (89 mg, 0.40 mmol) was added, and the mixture was stirred at room temperature for 10 hr. The reaction mixture was diluted with ethyl acetate (10 mL), and washed with saturated brine (10 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was purified by basic silica gel column chromatography (ethyl acetate/hexane=50/50→100/0), and the obtained solution was concentrated under reduced pressure. The residue was recrystallized from ethyl acetate to give the title compound (63 mg, 33%) as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697874B2
Source datasetuspto-grants-2014_04
ORD IDord-68a179a595244f25981fbd594ec36bf3
Source noteuspto-grants-2014_04