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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492725Generated: October 31, 2026

Ammonium Chloride → HCID 57677671, compound

https://huagongshe.com/reaction/492725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantTetrahydrofuran ethyl acetateHCID 21939870—
ReactantHCID 57677323HCID 57677323—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 57677671HCID 5767767194.2%

Reaction Steps

Piperidine-1-carboxylic acid [6-(2-fluoro-4-nitrophenoxy)pyrimidin-4-yl]amide (273 mg) was dissolved in ethanol (15 ml)-water (3 ml), and then electrolytic iron powder (275 mg) and ammonium chloride (550 mg) were added thereto, followed by heating under reflux for 30 min. The reaction mixture was cooled down to room temperature, and ethyl acetate-tetrahydrofuran (1:1) was then added thereto, followed by stirring. The reaction mixture was filtered through celite to remove an insoluble portion, which was washed with ethyl acetate and water. The organic layer of the filtrate was washed with water and brine in this order, and dried over anhydrous sodium sulfate. The solvent was evaporated under a reduced pressure to give a residue, which was then purified by silica gel column chromatography (Fuji Silysia NH, eluent; hexane:ethyl acetate=1:1 to 1:5). Fractions containing the target compound was concentrated under a reduced pressure, and dried in vacuum to provide the titled compound (235.8 mg, 94.1%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531532B2
Source datasetuspto-grants-2009_05
ORD IDord-a679ba567a9d484ab67cf995aa290862
Source noteuspto-grants-2009_05