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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255862Generated: October 30, 2026

Iodine → 6-Bromo-3-iodopyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/1255862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant6-Bromopyrazolo[1,5-a]pyrimidineHCID 22236701—
SolventAcetonitrileHCID 6342—
Product6-Bromo-3-iodopyrazolo[1,5-a]pyrimidineHCID 56845243—

Reaction Steps

A mixture of compound 6-bromopyrazolo[1,5-a]pyrimidine (1 eq), ceric ammonium nitrate (0.6 eq), and I2 (0.6 eq) in acetonitrile (10 mL) was stirred over a period of 24 h at room temperature. The formed precipitate was filtered off, washed with acetonitrile, and recrystallized from acetonitrile. The filtrate was evaporated, and the product was extracted with dichloromethane. The latter was evaporated, and the residue was recrystallized from acetonitrile to give 6-bromo-3-iodopyrazolo[1,5-a]pyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461162B2
Source datasetuspto-grants-2013_06
ORD IDord-fbf98b2bcc1e45488a6c9440734e81bf
Source noteuspto-grants-2013_06