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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181255Generated: November 3, 2026

Phosphorus oxychloride → HCID 11559938, compound

https://huagongshe.com/reaction/1181255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178517377HCID 178517377—
ProductHCID 11559938HCID 11559938—

Reaction Steps

A mixture of the above 5-cycloheptyl-6-(2,4,6-trifluorophenyl)imidazo[1,2-a]pyrimidin-7-ol (294 mg) in 2 mL of phosphorous oxychloride is heated at reflux for 6 h. The excess phosphorous oxychloride is removed in vaccuo, and the resulting residue is dissolved in methylene chloride. The organic layer is washed with water, dried over magnesium sulfate, and concentrated. The residue is chromatographed over silica gel, eluting with a gradient of 10% ethyl acetate in hexanes to 33% ethyl acetate in hexanes. Concentration provides 7-chloro-5-cycloheptyl-6-(2,4,6-trifluorophenyl)imidazo[1,2-a]pyrimidine as a white solid (24 mg). MS: m/z 380.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285555B2
Source datasetuspto-grants-2007_10
ORD IDord-f031efaba9e046a591d2101e45950647
Source noteuspto-grants-2007_10