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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107394Generated: October 31, 2026

Cyanogen Bromide → HCID 14032617, compound

https://huagongshe.com/reaction/2107394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 14032515HCID 14032515—
SolventChloroformHCID 6212—
ProductHCID 14032617HCID 1403261728.2%

Reaction Steps

A sample of 8.4 g of 1-benzoyl-3-(1-methyl-4-piperidinyl)-1H-indazole hydrochloride was converted to its free base and the base was dissolved in 135 ml of chloroform. The solution was stirred and 4.0 g of potassium carbonate was added followed by 2.7 g of cyanogen bromide. The reaction mixture was stirred under reflux for 16 hrs. The mixture was filtered, and the solvent was removed in vacuo. The mixture was chromatographed on a high-pressure column chromatography apparatus (silica gel), eluting with 0.3% methanol/dichloromethane. Evaporation of the appropriate fraction followed by recrystallization from toluene hexane yielded 2.2 g (28%) of the product, mp 144°-146° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04933460
Source datasetuspto-grants-1990_06
ORD IDord-2dd83283a4094040af9a00b4b2e43084
Source noteuspto-grants-1990_06