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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361812Generated: October 25, 2026

1-benzyl-N-methylpiperidin-4-amine → U 99363

https://huagongshe.com/reaction/361812

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-benzyl-N-methylpiperidin-4-amineHCID 4136128—
Reactant2-BROMO-3-ETHOXYPYRIDINEHCID 10631926—
SolventDichloromethaneHCID 6344—
ProductU 99363HCID 133107—

Reaction Steps

A mixture of 1-benzyl-4-(methylamino)piperidine (EXAMPLE 9, 2.92 g) and 2-bromo-3-ethoxypyridine (EXAMPLE 69, 1.44 g) is stirred at 160°-165° in a sealed tube for 2 days, diluted with methylene chloride (50 ml), washed with water (10 ml) and saline (10 ml), dried over sodium sulfate, and concentrated under reduced pressure. The residue is chromatographed on silica gel (230-400 mesh, 300 g; eluting with a gradient of ethyl acetate/hexane (10/90-50/50)) to give the title compound, C,H,N: Anal. Calcd for C20H27N3O1 : C=73.81, H=8.36, N=12.91-found: C=73.59, H=8.37, N=12.83.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866589
Source datasetuspto-grants-1999_02
ORD IDord-f46c67e942b3493db6a54f5c40fb808f
Source noteuspto-grants-1999_02