Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285496Generated: November 1, 2026

Pyridine → HCID 13338838, compound

https://huagongshe.com/reaction/1285496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHCID 13338836HCID 13338836—
SolventAcetic AcidHCID 176—
ProductHCID 13338838HCID 13338838—

Reaction Steps

A solution of 10.2 g (44.9 mmole) of 6-fluoro-5-(imidazol-1-yl)-2-methylquinoline, 16.7 g (180 mmole) of pyridine:diborane complex (that commercially available from Aldrich) and 200 ml of glacial acetic acid was stirred for about 22 hours at about 20° C. The solution was evaporated to reduce its volume, then 100 ml of 10% hydrochloric acid was added in small portions. The solution was heated on a steam bath for another one hour, then cooled with an ice bath and basified (pH 9 to 10) with 10% aqueous sodium hydroxide. The solid was separated by filtration, washed with water, and dissolved in ethyl acetate and dried. Recrystallization from aqueous ethanol provided 6-fluoro-5-(imidazol-1-yl)-1,2,3,4-tetrahydro-2-methylquinoline, m.p. 162°-164° C. Analysis: Calculated for C13H14FN3 : %C, 67.5; %H, 6.1; %N, 18.2; Found: %C, 67.5; %H, 6.1; %N, 18.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04567269
Source datasetuspto-grants-1986_01
ORD IDord-69681928dcce433b9d2e197e016f84b3
Source noteuspto-grants-1986_01