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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107383Generated: October 27, 2026

Water → 1-Ethyl-3-(1-methyl-4-piperidinyl)-1H-indazole hydrobromide

https://huagongshe.com/reaction/2107383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl BromideHCID 6332—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178480237HCID 178480237—
SolventDimethylformamideHCID 6228—
Product1-Ethyl-3-(1-methyl-4-piperidinyl)-1H-indazole hydrobromideHCID 1403249852.8%

Reaction Steps

To a stirred suspension of 0.86 g of sodium hydride (50% oil dispersion) in 50 ml of dimethylformamide was added, dropwise, 3.0 g of 3-(1-methyl-4-piperidinyl)-1H-indazole in 15 ml of hot dimethylformamide. The reaction mixture was stirred at ambient temperature and 1.34 ml of ethyl bromide in 10 ml of dimethylformamide was added, dropwise. The reaction was stirred overnight at ambient temperature and poured into water. The aqueous suspension was extracted with ethyl acetate (2X, 100 ml). The extracts were combined, washed with water, dried over anhydrous magnesium sulfate, and the solvent evaporated in vacuo to yield an oil. The oil was dissolved in a minimum amount of ethanol-ether, and a saturated solution of ether-hydrogen bromide was added. The salt was recrystallized from ethanol-ether to yield 2.4 g (52.8%) of product, mp 240°-242° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04933460
Source datasetuspto-grants-1990_06
ORD IDord-0d3afcdccd4e455983b38424f749c753
Source noteuspto-grants-1990_06