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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791265Generated: November 3, 2026

Thionyl Chloride → HCID 22030137, compound

https://huagongshe.com/reaction/1791265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 22030083HCID 22030083—
SolventDimethylformamideHCID 6228—
ProductHCID 22030137HCID 2203013793%

Reaction Steps

Heat a solution of 5′-nitro-3-trifluoromethyl-1′H[2,3′]bipyridinyl-6′-one (25 g, 0.088 mol), thionyl chloride (300 mL) and DMF (3 mL) to reflux for 4 hours. Remove the volatiles by rotary evaporation and partition the residue between ethyl acetate (350 mL) and saturated sodium bicarbonate solution (250 mL). Extract the aqueous layer with further ethyl acetate (250 mL) and wash the combined organics with brine (250 mL). Dry (MgSO4) and concentrate under reduced pressure to give the title compound (25 g, 93%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074799B2
Source datasetuspto-grants-2006_07
ORD IDord-3648be0c925346ff99a238ce1ea29109
Source noteuspto-grants-2006_07