Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398225Generated: October 30, 2026

Methanol → 4-chloro-6-phenyl-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/398225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactant7-Benzenesulfonyl-4-chloro6-phenyl-7H-pyrrolo[2,3-d]pyrimidineHCID 22484552—
SolventTetrahydrofuranHCID 8028—
Product4-chloro-6-phenyl-7H-pyrrolo[2,3-d]pyrimidineHCID 2248444276%

Reaction Steps

The product from Method D was dissolved in 10 mL of THF and to this solution was added 5.0 mL of methanol and 1.0 g of NaOH. The reaction mixture was stirred for 15 min., concentrated in vacuo and partitioned between a saturated aqueous solution of ammonium chloride (NH4Cl) and ethyl acetate. The resulting aqueous layer was extracted twice with ethyl acetate. The ethylacetate layers were combined, washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The crude product was purified by silica-gel chromatography (1:5 ethyl- acetate/hexane) to obtain 0.59 g (76%) of the title compound as a pale yellow solid, mp 145° C. (dec). LRMS: 230, 232 (M+2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610847B2
Source datasetuspto-grants-2003_08
ORD IDord-fea806bc400246cbace104dbb2a59874
Source noteuspto-grants-2003_08