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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2195673Generated: October 30, 2026

Dichloromethane → HCID 23149638, compound

https://huagongshe.com/reaction/2195673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantIsonicotinoyl chloride hydrochlorideHCID 12262826—
Reactant2-(3,4-Dihydroisoquinolin-2(1H)-yl)-5-(trifluoromethyl)anilineHCID 16769646—
SolventWaterHCID 962—
ProductHCID 23149638HCID 2314963897.6%

Reaction Steps

Isonicotinoyl chloride hydrochloride (390 mg, 2.19 mmol, commercially available product) and triethylamine (449 μl, 3.24 mmol) were sequentially added at 0° C. to a dichloromethane (5 ml) solution of 2-[2-amino-4-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydroisoquinoline (315 mg, 1.08 mmol), obtained as described in Referential Example 21-2. The resulting mixture was warmed to room temperature and stirred for half an hour. Water was added to the mixture, and the resulting mixture was extracted three times with dichloromethane. 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=2/1). Thus, N-[2-(1,2,3,4-tetrahydroisoquinolin-2-yl)-5-(trifluoromethyl)phenyl]isonicotinamide (GIF-0621) (418 mg, 97.6%) was yielded as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338362B2
Source datasetuspto-grants-2012_12
ORD IDord-81fd1a13ec64423f9068279c0c61bb38
Source noteuspto-grants-2012_12