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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 838848Generated: October 31, 2026

Iodine chloride → Pyrazolo(1.5-a)pyrimidine, 5,7-dimethyl-3-iodo-

https://huagongshe.com/reaction/838848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodine chlorideHCID 24640—
ReactantPyrazolo(1,5-a)pyrimidine, 5,7-dimethyl-HCID 215186—
SolventChloroformHCID 6212—
ProductPyrazolo(1.5-a)pyrimidine, 5,7-dimethyl-3-iodo-HCID 206164—

Reaction Steps

A solution of ICl [5.0g (27 mmoles)] in CHCl3 (50 ml) was added to a stirred solution of 5,7-dimethyl pyrazolo[1,5-a]pyrimidine [2.96g (20 mmoles)] in CHCl3 (50 ml). Within a few minutes, the mixture became warm and crystals of the hydrochloride salt of the subject compound began to separate. The mixture was warmed on the steam bath for 2-3 minutes to complete the reaction, and then refrigerated overnight. The yellow hydrochloride salt was separated by filtration, washed with Et2O, and air dried. The yellow solid, which weighed 4.4g, was dissolved in water (100 ml) and this solution was made alkaline by the addition of NaOH solution (2.5N). The alkaline solution was extracted with CHCl3 3(25 ml), and the CHCl3 extracts were dried over Na2SO4. The CHCl3 extract was chromatographed on basic alumina, and the CHCl3 eluant evaporated to dryness. The residue was recrystallized from petroleum ether (30°-60°) to afford 2.02g (37%) of analytically pure product; mp 120°-2°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04093617
Source datasetuspto-grants-1978_06
ORD IDord-8d8eada7a0e949ef9ded7f8dff1c40c2
Source noteuspto-grants-1978_06