Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852955Generated: October 31, 2026

Phosphorus oxychloride → HCID 86685297, compound

https://huagongshe.com/reaction/1852955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantDiisopropylethylamineHCID 81531—
Reactant7-(1-methyl-1H-pyrazol-4-yl)imidazo[1,2-c]pyrimidin-5(6H)-oneHCID 67451939—
ReactantMeOH DIEA EtOAcHCID 86685298—
SolventDichloromethaneHCID 6344—
ProductHCID 86685297HCID 8668529754.2%

Reaction Steps

To a suspension of 7-(1-methyl-1H-pyrazol-4-yl)imidazo[1,2-c]pyrimidin-5(6H)-one (Preparation I; 9.60 g, 44.6 mmol) in dry DCM (90 mL) was added DIEA and the suspension stirred at ambient temperature for 5 minutes. The mixture was cooled to 0° C. and POCl3 (12.3 mL, 134 mmol) was added over 5 minutes. The mixture was allowed to reach ambient temperature and the resulting thick slurry was treated with dry DCM (50 mL). The mixture was vigorously stirred at ambient temperature for 23 hours. The resulting light tan suspension was diluted with hexanes (90 mL) and collected by vacuum filtration. The collected solid was washed with Et2O and dried in vacuum to give the crude product salt. The salt was suspended in 5:20:75 MeOH/DIEA/EtOAc (200 mL) and stirred for 30 minutes at ambient temperature. The mixture was filtered through a SiO2 plug capped with a Celite layer eluting with 5% MeOH/EtOAc. The filtrate was concentrated and the residual solid dried in vacuum to provide the title compound (5.65 g, 54% yield) as a light cream colored solid. MS (apci) m/z=234.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962596B2
Source datasetuspto-grants-2015_02
ORD IDord-8b5b9c99bbf24882a11e3e6dd8fdd02f
Source noteuspto-grants-2015_02