Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044901Generated: October 30, 2026

Thionyl Chloride → 3-(Azidomethyl)-8-chloro-2-(5-fluoro-2-methoxyphenyl)quinoline

https://huagongshe.com/reaction/2044901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium AzideHCID 33557—
ReactantSodium borohydrideHCID 4311764—
Reactant8-Chloro-2-(5-fluoro-2-methoxyphenyl)quinoline-3-carbaldehydeHCID 57707922—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
Product3-(Azidomethyl)-8-chloro-2-(5-fluoro-2-methoxyphenyl)quinolineHCID 57707988—

Reaction Steps

To a stirred solution of 8-chloro-2-(5-fluoro-2-methoxyphenyl)quinoline-3-carb-aldehyde (385.4 mg, 1.221 mmol) in THF (6.0 mL) was added sodium borohydride (1.831 mmol) at rt. The solution was stirred 1 hour then diluted with water, and extracted with EtOAc to provide a crude solid after solvent removal, which was used without further purification. To the crude alcohol in CHCl3 (6 mL) was added thionyl chloride (0.445 mL, 6.103 mmol) at r.t. and stirred overnight. After 14 h the solvents were removed (TLC indicates complete.) The solid was dissolved in DMF (6 mL) then sodium azide (2.441 mmol) was added at once, and stirred 1 hour, poured into water and extracted EtOAc to give a crude material: 373.3 mg Chromatography, gradient 89/9/1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586739B2
Source datasetuspto-grants-2013_11
ORD IDord-cf78446dec744c2e93d0178216d332d3
Source noteuspto-grants-2013_11