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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112771Generated: November 2, 2026

Phosphorus oxychloride → HCID 59854770, compound

https://huagongshe.com/reaction/2112771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantChloro-N,N-dimethylformiminium chlorideHCID 77311—
ReactantSodium AcetateHCID 517045—
ReactantHCID 59854727HCID 59854727—
Solvent1,2-DichloroethaneHCID 11—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 59854770HCID 59854770—

Reaction Steps

POCl3 (3.5 ml) was added slowly to a cold, dry DMF (2.3 ml). 3-Benzyl-2-(3,4,5-trimethoxyphenyl)-6,7-dihydro-3H,5H-benzo[4,5]thieno[2,3-d]pyrimidine-4,8-dione (compound No. 2) (0.5 g, 1.1 mmol) in 1,2-dichloroethane was added slowly to the Vilsmeier reagent and stirred at room temperature for three hours after which the reaction mixture was refluxed for 15 minutes. After stirring overnight at room temperature the reaction mixture was diluted with dichloromethane and neutralized with NaOAc-solution (12 g/100 ml). The product was extracted with dichloromethane (3×30 ml). Organic phase was washed with water and dried. The crude product was purified by flash chromatography. The yield was 0.45 g (82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524853B2
Source datasetuspto-grants-2009_04
ORD IDord-6be380e7dbcf4942b9b3870da77466ac
Source noteuspto-grants-2009_04