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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252408Generated: October 26, 2026

Triethylamine → 3-Bromo-7-chloro-N-(1-hydroxycyclohexylmethyl)-4-quinolinamine

https://huagongshe.com/reaction/1252408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantBromineHCID 24408—
Reactant7-Chloro-N-[(1-hydroxycyclohexyl)methyl]-4-quinolinamineHCID 14209233—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product3-Bromo-7-chloro-N-(1-hydroxycyclohexylmethyl)-4-quinolinamineHCID 1420924449.2%

Reaction Steps

A solution of 11.2 g of 7-chloro-N-(1-hydroxycyclohexylmethyl)-4-quinolinamine in 130 ml of glacial acetic acid was stirred at room temperature and 6.15 g of bromine was added dropwise. The product precipitated from the solution as the hydrobromide salt and was isolated by filtration. The solid was then suspended in water and basified with sodium hydroxide. After two hours of stirring, the solid was collected by filtration. By combustion analysis, the product proved to be a hemi-hydrobromide salt, and therefore, it was necessary to dissolve the solid in methanol and 1 equivalent of trietylamine with heating. A solid resulted which was recrystallized from ethanol to give 7 g of crystalline solid with a melting point of 151°-154° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04743601
Source datasetuspto-grants-1988_05
ORD IDord-509a55169a9d4f9bb06f44b0dee29643
Source noteuspto-grants-1988_05