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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365837Generated: October 27, 2026

N,N-Dimethylaniline → 5,7-Dichloro-2-methylthiazolo[5,4-d]pyrimidine

https://huagongshe.com/reaction/1365837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantDichloromethaneHCID 6344—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2-methyl-4H-thiazolo[5,4-d]pyrimidine-5,7-dioneHCID 345642—
Product5,7-Dichloro-2-methylthiazolo[5,4-d]pyrimidineHCID 34563954%

Reaction Conditions

Temperature130 °C

Reaction Steps

To a mixture of 2-methyl-4H-thiazolo[5,4-d]pyrimidine-5,7-dione (7.5 g, 0.041 mol) in N,N-dimethylaniline (3.7 mL, 0.029 mol) was added phosphorous oxychloride (38.0 mL, 0.410 mol) and the mixture heated at 130° C. for 4 h. The resulting black solution was cooled to RT, then carefully quenched with crushed ice and H2O, before being extracted with EtOAc. The organic layer was isolated, dried (MgSO4) and concentrated in vacuo to give a yellow solid. The solid was dissolved in DCM, then washed with an aqueous solution of NaHCO3 followed by brine, dried (Na2SO4) and concentrated in vacuo to give the title compound as a pale yellow solid (4.90 g, 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893060B2
Source datasetuspto-grants-2011_02
ORD IDord-114f9f6f779a4fe79604625ef0e7b07c
Source noteuspto-grants-2011_02