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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175562Generated: November 1, 2026

Tetrahydrofuran → Tert-butyl 2-((2-carbamoyl-6-(trifluoromethyl)quinolin-4-yl)amino)acetate

https://huagongshe.com/reaction/2175562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTert-butyl 2-(2-cyano-6-(trifluoromethyl)quinolin-4-ylamino)acetateHCID 58562608—
SolventEthanolHCID 702—
ProductTert-butyl 2-((2-carbamoyl-6-(trifluoromethyl)quinolin-4-yl)amino)acetateHCID 68003428—

Reaction Conditions

Temperature75 °C

Reaction Steps

A solution of tert-butyl 2-((2-cyano-6-(trifluoromethyl)quinolin-4-yl)amino)acetate (329 mg, 0.94 mmol) from above step A, in EtOH (3 mL) water (600 uL) and THF (5 mL) was added hydrido(dimethylphosphinous acid-kp)[hydrogen bis(dimethylphosphinito-kp)]platinum(ii) (80 mg, 0.18 mmol) and stirred at 75° C. for 3 h. The mixture was filtered to remove the white solid that had formed and the filtrate was evaporated under vacuum. The residue was purified by silica column chromatography to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062048B2
Source datasetuspto-grants-2015_06
ORD IDord-7ee7e9be858846d4949d4ddd94f15957
Source noteuspto-grants-2015_06