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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805849Generated: October 30, 2026

Tert-Butyl nitrite → 2,4-Dichloro-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/1805849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-Butyl nitriteHCID 10906—
ReactantAntimony trichlorideHCID 24814—
Reactant4-chloro-7H-pyrrolo(2,3-d)pyrimidin-2-amineHCID 5324413—
Solvent1,2-DichloroethaneHCID 11—
SolventChloroformHCID 6212—
Product2,4-Dichloro-7H-pyrrolo[2,3-d]pyrimidineHCID 1411687143%

Reaction Steps

To a suspension of 4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-ylamine (500 mg, 2.97 mmol) in 1,2-dichloroethane (40 mL) at −10° C. under argon was added antimony chloride (750 mg, 3.29 mmol). After stirring for 5 min, tert-butylnitrite (2.50 mL, 20.8 mmol) was added to the solution. The reaction was stirred at −10° C. for 3 h. The reaction was diluted with CHCl3 (100 mL) and poured into ice water (50 mL). The CHCl3 layer was separated, washed with brine (20 mL), dried with Na2SO4, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=50:50) yielded 239 mg (43%) of 2,4-dichloro-7H-pyrrolo[2,3-d]pyrimidine as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354532B2
Source datasetuspto-grants-2013_01
ORD IDord-043e88357cbb4916b8a6324b66b8f7c5
Source noteuspto-grants-2013_01