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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845611Generated: October 25, 2026

Sodium hydride → 1-Cyclopropylmethyl-3-(1-methyl-4-piperidinyl)-1H-indazole hydrobromide

https://huagongshe.com/reaction/845611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant(Chloromethyl)cyclopropaneHCID 80013—
ReactantEther hydrobromideHCID 86739792—
ReactantHCID 178480237HCID 178480237—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product1-Cyclopropylmethyl-3-(1-methyl-4-piperidinyl)-1H-indazole hydrobromideHCID 1403250932%

Reaction Steps

To a stirred mixture of 1.19 g of sodium hydride (50% oil dispersion) in 65 ml of dimethylformamide was added, dropwise, 4.0 g of 3-(1-methyl-4-piperidinyl)-1H-indazole in 20 ml of hot dimethylformamide. The mixture was stirred for 1 hr at ambient temperature and then 1.40 g of chloromethylcyclopropane in 10 ml of dimethylformamide was added dropwise. The reaction mixture was stirred for 21/2 days at ambient temperature. The reaction mixture was quenched with water, extracted with ethyl acetate, washed with water, dried over anhydrous magnesium sulfate and the solvent was removed in vacuo to yield an oil. The oil was dissolved in ether and saturated hydrogen bromide/ether solution was added dropwise to precipitate a salt. The salt was recrystallized from toluene and ethyl acetate to yield 2.8 g (32%) of product, mp 177°-179° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04758668
Source datasetuspto-grants-1988_07
ORD IDord-322c4323acd8466fa6f1b738e4cf4cb3
Source noteuspto-grants-1988_07