Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184584Generated: October 30, 2026

Chloroacetonitrile → HCID 178511314, compound

https://huagongshe.com/reaction/2184584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetonitrileHCID 7856—
ReactantDichloromethane ethylacetateHCID 21226138—
ReactantHCID 178505426HCID 178505426—
SolventAcetonitrileHCID 6342—
ProductHCID 178511314HCID 17851131489.1%

Reaction Steps

To a stirred suspension of 4-(6-fluoro-1H-indazol-3-yl)piperidine (4.95 g, 22.6 mmol) and NaHCOa (2.1 g, 24.9 mmol) in dry acetonitrile (110 ml) was added chloroacetonitrile (1.6 ml, 24.9 mmol) at room temperature, under nitrogen. The suspension was warmed to reflux for 22.5 hours, cooled to room temperature, and subsequently filtered. The remaining solids were washed with DCM and the combined filtrates were concentrated. The resulting brown oil was dissolved into EtOAc and washed with water. The organic phase was dried (MgSO4), filtered and concentrated to give a brown solid which was re-dissolved into DCM/EtOAc and flushed through alumina with DCM. The eluent was concentrated to give 5.2 g of the desired product as a solid, m.p. 149°-151° C. ANALYSIS: Calculated for C14H15FN4: 65.10%C 5.85%H 21.69%N Found: 64.84%C 5.90%H 21.74%N

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037729E1
Source datasetuspto-grants-2002_06
ORD IDord-e51e7bf4bf4c4c11ade2aba39499ef84
Source noteuspto-grants-2002_06