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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501437Generated: October 25, 2026

Hexachloroethane → 3-(2-Butynyl)-2,4-dichloro-3H-imidazo[4,5-c]pyridine

https://huagongshe.com/reaction/501437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexachloroethaneHCID 6214—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium diisopropylamideHCID 2724682—
Reactant3-(2-Butynyl)-4-chloro-3H-imidazo[4,5-c]pyridineHCID 23070729—
SolventTetrahydrofuranHCID 8028—
Product3-(2-Butynyl)-2,4-dichloro-3H-imidazo[4,5-c]pyridineHCID 2307098021%

Reaction Steps

2.22 ml of a tetrahydrofuran solution of lithium diisopropylamide was added dropwise to a 5 ml tetrahydrofuran solution of 490 mg of 3-(2-butynyl)-4-chloro-3H-imidazo[4,5-c]pyridine in a dry ice-methanol bath, and the mixture was stirred below −66° C. for 20 minutes. The resulting reaction mixture was added dropwise to a 2 ml tetrahydrofuran solution of 1.13 g of hexachloroethane while the temperature of the mixture was controlled to be −63° C. or lower. The mixture was stirred for one hour and 40 minutes in the same bath, and then a saturated aqueous ammonium chloride solution was added thereto. The resulting mixture was extracted twice with ethyl acetate, and the organic layer was dried over anhydrous magnesium sulfate, then filtered. The filtrate was concentrated under reduced pressure. Then, the resulting residue was purified by silica gel column chromatography. Thus, 120 mg of brown oily material was obtained from the fraction eluted with hexane-ethyl acetate (2:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772226B2
Source datasetuspto-grants-2010_08
ORD IDord-8adadceae381408d99ea7a971222e9dd
Source noteuspto-grants-2010_08