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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108778Generated: October 31, 2026

Phosphorus oxychloride → HCID 178478399, compound

https://huagongshe.com/reaction/1108778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178518716HCID 178518716—
ProductHCID 178478399HCID 17847839949%

Reaction Steps

A mixture of 1,3-azaphospholo[4,5-d]pyrimidin-7(1H,6H)-one (compound 12, 5.0 g, 32.66 mmol) and phosphorus oxychloride (125 mL) was heated under reflux with stirring for 50 min under an argon atmosphere. The reaction mixture was cooled to room temperature and unreacted phosphorus oxychloride was removed under reduced pressure at 25° C. The residual syrup was cooled to 0° C. and carefully neutralized with 2 N aqueous ammonium hydroxide. The precipitate formed was collected by filtration, washed with cold water (2×25 mL) and dried over P2O5 under vacuum, first at 25° C. and then at 100° C. The dry solid was crystallized from acetonitrile to yield 2.73 g (49%) of the title compound, mp>300° C. (became black at 190° C.). 1H nmr (DMSO-d6): δ 8.81 (s, 1 H, C5H), 9.36 (dd, 1 H, JC2H, NH =4.8 Hz, JC2H,P =39.4 Hz, C2H), and 13.68 (br s, 1 H, NH). Anal. Calcd. for C5H3ClN3P: C, 35.02; H, 1.76; Cl, 20.67; N, 24.50; P, 18.05. Found: C, 35.36; H, 2.08; Cl, 21.10; N, 24.21; P, 17.78.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06069132
Source datasetuspto-grants-2000_05
ORD IDord-0bad3cf92fdd4afc8eca0c48a087d543
Source noteuspto-grants-2000_05