Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426011Generated: October 27, 2026

N-Methyl-2-piperidone → HCID 66703723, compound

https://huagongshe.com/reaction/426011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methyl-2-piperidoneHCID 13603—
ReactantL-AlaninolHCID 80307—
Reactant2-fluoro-N-(1-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-7-yl)-4-(trifluoromethyl)benzamideHCID 66703605—
ProductHCID 66703723HCID 6670372365.4%

Reaction Conditions

Temperature180 °C

Reaction Steps

2-Fluoro-N-(1-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-7-yl)-4-(trifluoromethyl)benzamide (250 mg), N-methylpiperidone (0.5 mL) and (2S)-2-aminopropan-1-ol (800 mg) were mixed, followed by stirring at 180° C. for 40 minutes under microwave irradiation. After spontaneous cooling and subsequent purification by silica gel column chromatography (chloroform:methanol, 99:1 to 95:5), 2-{[(1S)-2-hydroxy-1-methylethyl]amino}-N-(1-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-7-yl)-4-(trifluoromethyl)benzamide (188 mg) was obtained as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106190B2
Source datasetuspto-grants-2012_01
ORD IDord-43b19f486fa8451db8f3e66a00599959
Source noteuspto-grants-2012_01