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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270014Generated: November 1, 2026

Chloroacetonitrile → [4-(1H-Indazol-3-yl)1-piperazinyl]acetonitrile

https://huagongshe.com/reaction/2270014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetonitrileHCID 7856—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(Piperazin-1-YL)-1H-indazoleHCID 14823445—
SolventAcetonitrileHCID 6342—
Product[4-(1H-Indazol-3-yl)1-piperazinyl]acetonitrileHCID 1846729155.8%

Reaction Steps

To a stirred suspension of 3-piperazin-1-yl-1H-indazole (6.0 g, 29.7 mmol) and NaHCO3 (2.7 g, 32.7 mmol) in dry acetonitrile (125 ml) was added chloroacetonitrile (2.1 ml, 31.2 mmol) at room temperature, under nitrogen. The suspension was warmed to reflux for 17.5 hours, cooled to room temperature, and subsequently filtered. The remaining solids were washed with dichloromethane and the combined filtrates were concentrated. The resulting brown oil was purified via flash column chromatography (silica gel, 0-50% EtOAc/DCM) to give 4.0 g of product as an off-white solid, m.p. 121°-123° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037478E1
Source datasetuspto-grants-2001_12
ORD IDord-4890f2413cf84fab9a1fbbf271c0ba1d
Source noteuspto-grants-2001_12