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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678236Generated: October 26, 2026

Phosphorus oxychloride → 4-chloro-7H-pyrrolo(2,3-d)pyrimidin-2-amine

https://huagongshe.com/reaction/1678236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178508865HCID 178508865—
Product4-chloro-7H-pyrrolo(2,3-d)pyrimidin-2-amineHCID 5324413—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 2-amino-7H-pyrrolo[2,3-d]pyrimidin-4-ol (Sigma, 150 mg, 1.0 mmol) in phosphorus oxychloride (1.5 mL) was heated at about 110° C. for about 30 minutes. Phosphorus oxychloride was carefully removed under reduced pressure and the reaction mixture was quenched by slow addition of ice water (10 mL). The resulting mixture was neutralized with saturated aqueous sodium carbonate (about 5 mL) to pH 7. The crude product was extracted into dichloromethane (20 mL) and washed with water (15 mL). The organic layer was separated and the aqueous phase was further extracted with dichloromethane (3×30 mL). The combined organic extracts were dried over anhydrous sodium sulfate and concentrated to give 4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-ylamine (0.036 g, 0.21 mmol) as a light yellow solid; LC/MS (Table 1, Method a) Rt 1.17 min; MS m/z: (M+H)+ 169.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008481B2
Source datasetuspto-grants-2011_08
ORD IDord-749f6d8f51ba451a832b255b914fd685
Source noteuspto-grants-2011_08