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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742958Generated: October 27, 2026

Ammonia → Methyl 4-amino-1-benzyl-1,2,5,6-tetrahydropyridine-3-carboxylate

https://huagongshe.com/reaction/742958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSodium CarbonateHCID 10340—
ReactantMethyl 1-benzyl-4-oxopiperidine-3-carboxylate hydrochlorideHCID 107479—
SolventEthanolHCID 702—
ProductMethyl 4-amino-1-benzyl-1,2,5,6-tetrahydropyridine-3-carboxylateHCID 563385—

Reaction Steps

855 g of methyl 1-benzyl-4-oxopiperidine-3-carboxylate hydrochloride, 176 g of sodium carbonate and 450 ml of 25% aqueous ammonia solution in 6.5 1 of ethanol were heated for 5 h at an internal temperature of 70° C., with stirring. After concentration under reduced pressure, the mixture was worked up by extraction with dichloromethane and water. The combined dichloromethane phases were dried over sodium sulfate and concentrated under reduced pressure to give 788 g of oily methyl 4-amino-1-benzyl-1,2,5,6-tetrahydropyridine-3-carboxylate as a crude product, which was used in Example 1b) without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556854
Source datasetuspto-grants-1996_09
ORD IDord-9e06aeec1ce64a15a8b4388b7277b47c
Source noteuspto-grants-1996_09