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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252193Generated: October 30, 2026

Dichloromethane → HCID 66846503, compound

https://huagongshe.com/reaction/252193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant3-(Trifluoromethyl)benzoyl chlorideHCID 75257—
ReactantHCID 59860302HCID 59860302—
SolventEthyl AcetateHCID 8857—
ProductHCID 66846503HCID 66846503—

Reaction Steps

To a solution of 3-(3-amino-2,6-dichloro-phenyl)-[1,6]naphthyridin-2-ylamine (2.0 g, 6.554 mmol) in the dichloromethane (400.0 mL) is added 3-(trifluoromethyl)benzoyl chloride (4.78 g, 22.94 mmol). After the mixture is stirred for 24 hours at room temperature, it is diluted with EtOAc and washed with saturated K2CO3, brine and water. The organic layer is dried, filtered and concentrated to give crude product, which is purified by flash silica gel column eluting with CH2Cl2 (100%) gradient to CH2Cl2/MeOH (NH3, 2N) (95/5) to give the product as a solid: 1H NMR 400 MHz (CDCl3) δ 8.97 (s, 1H), 8.61 (d, 1H), 8.57 (d, 1H), 8.52 (s, 1H), 8.20 (s, 1H), 8.06 (d, 1H), 7.86 (d, 1H), 7.85 (s, 1H), 7.68 (t, 1H), 7.58 (d, 1H), 7.51 (d, 3H), 5.25 (s, 2H); MS m/z 478.10 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868018B2
Source datasetuspto-grants-2011_01
ORD IDord-728385908b6d4efa92701899b50b2250
Source noteuspto-grants-2011_01