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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249720Generated: November 1, 2026

tert-Butyl 4-formylpiperidine-1-carboxylate → HCID 18328903, compound

https://huagongshe.com/reaction/1249720

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantPyrimidine, 2-methyl-4-(1-piperazinyl)-, hydrochloride (1:2)HCID 18328942—
SolventAcetic acid methanolHCID 10129899—
ProductHCID 18328903HCID 1832890324.1%

Reaction Steps

To a solution of 1-(tert-butoxycarbonyl)-4-(formyl)piperidine (7.14 g) and 1-(2-methylpyrimidin-4-yl)piperazine dihydrochloride (8.38 g) in methanol/acetic acid (99:1) (150 ml) was added sodium cyanoborohydride (6.32 g) portionwise over 30 minutes and the resultant suspension stirred at arnbient temperature for 3 hours. The suspension was quenched by addition of saturated aqueous sodium bicarbonate solution and the resulting mixture extracted with ethyl acetate. The organic phase was dried (Na2SO4) and evaporated. The residue was purified by chromatography eluting with 5% methanol in dichloromethane to give 1-tert-butoxycarbonyl-4-[1-(2-methylpyrimidin-4-yl)piperazin-4-ylmethyl]piperidine (3.02 g) as a foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06335341B1
Source datasetuspto-grants-2002_01
ORD IDord-0ab5f0d385e94395a29e5583357d3447
Source noteuspto-grants-2002_01