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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450397Generated: October 31, 2026

Chlorosuccinimide → 3,7-Dichloro-5-ethylpyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/1450397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactant7-Chloro-5-ethylpyrazolo[1,5-a]pyrimidineHCID 10535410—
SolventChloroformHCID 6212—
Product3,7-Dichloro-5-ethylpyrazolo[1,5-a]pyrimidineHCID 10632484—

Reaction Steps

5.5 g (30 mmol) of the chloro compound (Example 1, Step B) and 4.0 g (30 mmol) of N-chlorosuccinimide were dissolved in 150 ml chloroform, stirred for 4 h at room temperature, and finally heated for some minutes on a steam bath. The mixture was poured on to ice water, the aqueous layer extracted with dichloromethane, the combined organic layers washed twice with saturated sodium carbonate solution, dried over sodium sulfate, and evaporated in in vacuo. The title compound was obtained as an oil after chromatography on silica gel with dichlormethane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05602136
Source datasetuspto-grants-1997_02
ORD IDord-c7658f54bd3849a2b4b805da9f8b1209
Source noteuspto-grants-1997_02