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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270706Generated: October 31, 2026

3-(Trifluoromethyl)benzoyl chloride → HCID 59833927, compound

https://huagongshe.com/reaction/270706

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)benzoyl chlorideHCID 75257—
ReactantPyrido[2,3-d]pyrimidin-7-amine,6-(3-amino-2,6-dichlorophenyl)-2-(methylthio)-HCID 59860298—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 59833927HCID 5983392779.4%

Reaction Steps

To a solution of 6-(3-amino-2,6-dichloro-phenyl)-2-methylsulfanyl-pyrido[2,3-d]-pyrimidin-7-ylamine (0.5 g, 1.42 mmol) in CH2Cl2 (40 mL) is added 3-(trifluoromethyl)benzoyl chloride (1.07 mL, 7.1 mmol). After the mixture is stirred for 24 hours at room temperature, the mixture 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 a flash silica gel column, eluting with CH2Cl2 (100%) gradient to CH2Cl2/MeOH(NH3, 2N)(95/5%), to give the title intermediate as a solid (0.591 g, 79.4 %).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449582B2
Source datasetuspto-grants-2008_11
ORD IDord-bde1a0e0b70746c79aebdd217ba2e11b
Source noteuspto-grants-2008_11