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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881419Generated: November 2, 2026

Methylamine → tert-Butyl 4-(methylamino)piperidine-1-carboxylate

https://huagongshe.com/reaction/881419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 4-(methylamino)piperidine-1-carboxylateHCID 1538070246%

Reaction Steps

To a solution of 1-BOC-4-piperidone (3.5 g, 17.5 mmol) in methanol (10 mL) was added a solution of 2M methylamine in methanol (13 mL, 26 mmol). The reaction mixture was stirred for 16 hours and then sodium cyanoborohydride (1.1 g, 17.5 mmol) was added. After stirring for 2 hours the reaction mixture was then diluted with dichloromethane, washed with sodium bicarbonate solution, dried (MgSO4) and the solvent removed in vacuo. The residue was purified by flash chromatography using 10% methanol in dichloromethane as the eluent to yield 4-methylamino-piperidine-1-carboxylic acid tert-butyl ester (1.72 g, 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993563B2
Source datasetuspto-grants-2015_03
ORD IDord-42fb4ad19d1b4c45adac0de351912dd4
Source noteuspto-grants-2015_03