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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091693Generated: November 1, 2026

2-(chloromethyl)-6-methyl-5-phenyl-3H,4H-thieno(2,3-d)pyrimidin-4-one → 1-((6-Methyl-4-oxo-5-phenyl-3,4-dihydrothieno[2,3-d]pyrimidin-2-yl)methyl)-3-(trifluoromethyl)-1H-pyrazole-4-carbaldehyde

https://huagongshe.com/reaction/1091693

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(chloromethyl)-6-methyl-5-phenyl-3H,4H-thieno(2,3-d)pyrimidin-4-oneHCID 2393069—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178519884HCID 178519884—
SolventTetrahydrofuranHCID 8028—
Product1-((6-Methyl-4-oxo-5-phenyl-3,4-dihydrothieno[2,3-d]pyrimidin-2-yl)methyl)-3-(trifluoromethyl)-1H-pyrazole-4-carbaldehydeHCID 8663039838.1%

Reaction Steps

To a stirred suspension of 3-(trifluoromethyl)-1H-pyrazole-4-carbaldehyde (100 mg, 0.609 mmol) and potassium tert-butoxide (137 mg, 1.22 mmol) in THF (3 mL) was added 2-(chloromethyl)-6-methyl-5-phenylthieno[2,3-d]pyrimidin-4(3H)-one (177 mg, 0.609 mmol) and the resultant solution was stirred at RT for 2 days. The reaction mixture was quenched with water and concentrated in vacuo to give the crude product as a beige solid (97 mg, 0.232 mmol, 38%). The material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129397B2
Source datasetuspto-grants-2012_03
ORD IDord-123a114657704bcfae729ff0f0561ac8
Source noteuspto-grants-2012_03