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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908609Generated: October 30, 2026

Phosphorus oxychloride → 2,7-Dichloro-5-cyclopropyl-thiazolo[4,5-d]pyrimidine

https://huagongshe.com/reaction/908609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178517401HCID 178517401—
Product2,7-Dichloro-5-cyclopropyl-thiazolo[4,5-d]pyrimidineHCID 59703762—

Reaction Steps

To a solution of the compound (0.82 g) obtained in Step 4 in phosphorus oxychloride (2.5 ml) was added N,N-diisopropylethylamine (0.25 ml) under ice-cooling, and the mixture was heated under reflux for 2 hr. The reaction mixture was concentrated under reduced pressure, toluene was added to the residue, and the mixture was concentrated again under reduced pressure. The obtained residue was dissolved in ethyl acetate, poured into ice water and partitioned. The organic layer was washed successively with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous sodium sulfate, filtrated, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:n-hexane=1:8) to give the title compound (0.79 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017612B2
Source datasetuspto-grants-2011_09
ORD IDord-964db4f1b44c4406afb175ce02e30b31
Source noteuspto-grants-2011_09