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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410305Generated: November 2, 2026

Dichloromethane → HCID 17402881, compound

https://huagongshe.com/reaction/2410305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
Reactant2-(Piperidin-1-yl)anilineHCID 458795—
ReactantIsonicotinoyl chloride hydrochlorideHCID 12262826—
SolventWaterHCID 962—
ProductHCID 17402881HCID 17402881—

Reaction Steps

Isonicotinoyl chloride hydrochloride (616 mg, 3.46 mmol, commercially available product) and triethylamine (800 μl, 5.73 mmol) were sequentially added at 0° C. to a dichloromethane (5 ml) solution of 2-(1-piperidinyl)aniline (203 mg, 1.15 mmol), obtained as described in Referential Example 18-2. The resulting mixture was warmed to room temperature and stirred for two hours. Water was added to the mixture, and the resulting mixture was extracted three times with ethyl acetate. The obtained organic layer was washed with a saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (20 g, hexane/ethyl acetate=1/1). Thus, N-[2-(1-piperidinyl)phenyl]isonicotinamide (GIF-0349) (259 mg, 80.0%) was yielded as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816089B2
Source datasetuspto-grants-2014_08
ORD IDord-95b29ab87e8c4f86a5337c6503ba4526
Source noteuspto-grants-2014_08