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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934415Generated: November 2, 2026

Phosphorus oxychloride → HCID 178435385, compound

https://huagongshe.com/reaction/1934415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178435422HCID 178435422—
ProductHCID 178435385HCID 17843538567%

Reaction Steps

A solution of 3.35 g (20.5 mmol) of 1,7-dihydro-6-ethyl-4H-pyrrolo[2,3-d]pyrimidin-4-one in 187 mL of phosphorous oxychloride was heated to reflux for 4 hours. The reaction was cooled to ambient temperature and concentrated under vacuum. The residue was dissolved in 100 mL of methylene chloride and poured onto 100 g of ice. The mixture was neutralized to pH 7 by the addition of powdered potassium carbonate. After an additional 200 mL of methylene chloride and 200 mL of water were added, some solids remained and were removed by filtration. The solids were shown to be desired product by thin layer chromatography (silica, 19:1 methylene chloride-methanol). The solids were combined with the organic phase and concentrated to 4.0 g of brown residue. The residue was purified by flash chromatography (200 g of silica, 19:1 methylene chloride-methanol) to provide 2.50 g (67%) of 4-chloro-6-ethyl-1H-pyrrolo[2,3-d]pyrimidine as a white solid. nmr (500 MHz, dmso-d6) δ1.27 (t, J=7.5 Hz, 3H), 2.76 (q, J=7.5 Hz, 2H), 6.30 (s, 1H), 8.48 (s, 1H), 12.41 (s, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384041B1
Source datasetuspto-grants-2002_05
ORD IDord-e62bfdaab9384b3f97966b1e47dfb4ef
Source noteuspto-grants-2002_05