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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242040Generated: October 26, 2026

3-Fluorobenzylamine → HCID 56847340, compound

https://huagongshe.com/reaction/242040

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-FluorobenzylamineHCID 66853—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 66584532HCID 66584532—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventAcetone hexaneHCID 21880519—
ProductHCID 56847340HCID 5684734057%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 280 mg (0.79 mmol) 4-methyl-2-oxo-1-(tetrahydro-2H-pyran-4-yl)-7-(trifluoromethyl)-1,2-dihydroquinoline-3-carboxylic acid in DCM (5 ml) were added 360 mg (0.95 mmol) HATU and 54 μl (3.15 mmol) DIPEA at 0° C. The reaction mixture was stirred for 5 min at 0° C. followed by the addition of 90 μl (0.79 mmol) 3-fluoro-benzylamine. The reaction mixture was stirred at RT for 4 h. Then the mixture was diluted with water (5 ml) and extracted with DCM (3×10 ml). The combined organic layers were washed with water (10 ml), brine (10 ml), dried over anhydrous Na2SO4 and concentrated in vacuum. After CC (acetone/hexane 1:3) of the residue, 210 mg (0.45 mmol, 57%) N-[(3-fluorophenyl)-methyl]-4-methyl-2-oxo-1-tetrahydro-pyran-4-yl-7-(trifluoromethyl)-1H-quinoline-3-carboxylic acid amide (example 44) were obtained. MS: m/z 463.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653102B2
Source datasetuspto-grants-2014_02
ORD IDord-1f7468e3ba8e4c68908f062e4fa731bc
Source noteuspto-grants-2014_02