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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469814Generated: October 31, 2026

Dimethylformamide → 2-Chloro-5-(pivalamidomethyl)-N-(8-((3-(trifluoromethyl)phenyl)amino)quinolin-4-yl)benzamide

https://huagongshe.com/reaction/1469814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant4-Nitrophenyl 2-chloro-5-(pivalamidomethyl)benzoateHCID 86692238—
ReactantN-(3-(trifluoromethyl)phenyl)quinoline-4,8-diamineHCID 86692281—
Product2-Chloro-5-(pivalamidomethyl)-N-(8-((3-(trifluoromethyl)phenyl)amino)quinolin-4-yl)benzamideHCID 86692280—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a solution of N-(3-(trifluoromethyl)phenyl)quinoline-4,8-diamine (Intermediate-12, 80 mg, 0.264 mmol) in DMF (2 mL) was added NaH (26 mg, 0.65 mmol, 60% in mineral oil) at 0° C. and the reaction mixture was stirred at 0-5° C. for 30 minutes. Then a solution of 4-nitrophenyl 2-chloro-5-(pivalamidomethyl)benzoate (Intermediate-13, 123 mg, 0.314 mmol) in DMF (1 mL) was added to the reaction mixture at 0° C. and the reaction mixture was stirred at 0° C.—rt for 2 h. Then the reaction mixture was quenched with water and was extracted with EtOAc. The organic layer was washed with brine, separated, dried, filtered and concentrated. The residue was purified by column chromatography to afford 15 mg of the title product. 1H NMR (300 MHz, DMSO-d6): δ 10.92 (s, 1H), 9.07 (s, 1H), 8.86 (d, J=4.8 Hz, 1H), 8.21-8.18 (m, 2H), 7.80-7.57 (m, 3H), 7.59-7.54 (m, 5H), 7.39 (d, J=8.4 Hz, 1H), 7.25 (d, J=7.2 Hz, 1H), 4.32 (d, J=6.0 Hz, 2H), 1.19 (s, 9H); MS [M+H]+: 555.25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006257B2
Source datasetuspto-grants-2015_04
ORD IDord-6bafbb161c4f4c8f91ccf29b45c45746
Source noteuspto-grants-2015_04