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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532470Generated: October 30, 2026

Tetrahydrofuran → 7-bromo-4-chloro-5H-pyrrolo[3,2-d]pyrimidine

https://huagongshe.com/reaction/532470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantN-bromobutanimideHCID 67184—
Reactant4-chloro-5H-pyrrolo[3,2-d]pyrimidineHCID 5370695—
SolventEthyl AcetateHCID 8857—
Product7-bromo-4-chloro-5H-pyrrolo[3,2-d]pyrimidineHCID 52987660—

Reaction Steps

To 4-chloro-5H-pyrrolo[3,2-d]pyrimidine (100 mg), tetrahydrofuran (5 mL) was added, and N-bromosuccinimide (116 mg) was further added thereto, followed by stirring for 1 hour. After completion of the reaction, the reaction mixture was mixed with ethyl acetate and washed with water. The washed mixture was dried over anhydrous sodium sulfate, and filtered and distilled under reduced pressure to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853213B2
Source datasetuspto-grants-2014_10
ORD IDord-cf21458fd1b4488ebd2201ecfae11a77
Source noteuspto-grants-2014_10