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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366788Generated: November 2, 2026

p-(Trifluoromethoxy)phenyl isocyanate → HCID 58451290, compound

https://huagongshe.com/reaction/2366788

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-(Trifluoromethoxy)phenyl isocyanateHCID 92298—
ReactantN-[5-(3-amino-4-fluorophenoxy)[1,3]thiazolo[5,4-b]pyridin-2-yl]cyclopropanecarboxamideHCID 86646022—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 58451290HCID 5845129074%

Reaction Conditions

Temperature70 °C

Reaction Steps

N-[5-(3-Amino-4-fluorophenoxy)[1,3]thiazolo[5,4-b]pyridin-2-yl]cyclopropanecarboxamide (150 mg, 0.44 mmol) was dissolved in pyridine (3.0 mL), 1-isocyanato-4-(trifluoromethoxy)benzene (99 μL, 0.66 mmol) was added, and the mixture was stirred at 70° C. for 2 hr. 1-Isocyanato-4-(trifluoromethoxy)benzene (20 μL, 0.13 mmol) was added to the reaction mixture, and the mixture was further stirred at 70° C. for 3 hr. The obtained suspension was cooled to room temperature, and diluted with ethyl acetate (5 mL), tetrahydrofuran (1 mL) and n-hexane (5 mL). The precipitated resultant product was collected by filtration to give the title compound (177 mg, 74%) as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697874B2
Source datasetuspto-grants-2014_04
ORD IDord-cd45abc82cdb4097937e6b48aaa5633d
Source noteuspto-grants-2014_04