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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743075Generated: October 30, 2026

Water → HCID 11516226, compound

https://huagongshe.com/reaction/743075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 19423566HCID 19423566—
SolventEthanolHCID 702—
ProductHCID 11516226HCID 11516226—
ProductHCID 11516277HCID 11516277—

Reaction Steps

To a solution of 18.0 g (34.9 mmol) of 3-[α-{(1-benzylpiperidin-4-yl)imino}benzyl]-4-trichloroacetylaminopyridine in 150 mL of ethanol was added 2.65 g (70 mmol) of sodium borohydride under ice-cooling and the mixture was stirred for 5 hours at ambient temperature. The reaction mixture was poured into water, and the ethanol was evaporated in vacuo. The residue was extracted with ethyl acetate. The organic layer separated was washed with water and then with brine, dried on anhydrous sodium sulfate and then concentrated in vacuo. Purification by means of column chromatography (silica gel, 1:9 methanol:chloroform) gave 4.82 g (12.9 mmol) of the title compound and 6.65 g (17.9 mmol) of 3-[α-{(1-benzyl-piperidin-4-yl)imino}benzyl]-4-aminopyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556860
Source datasetuspto-grants-1996_09
ORD IDord-0b0bd4d1bbf34a429811ba0d7e473c53
Source noteuspto-grants-1996_09