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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842327Generated: November 3, 2026

2-Bromopropane → HCID 57494028, compound

https://huagongshe.com/reaction/1842327

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropaneHCID 6358—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl 4-[(2-methoxyethyl)amino]piperidine-1-carboxylateHCID 43652134—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 57494028HCID 57494028—

Reaction Conditions

Temperature60 °C

Reaction Steps

Amine preparation: A mixture of 4-(2-methoxy-ethylamino)-piperidine-1-carboxylic acid tert-butyl ester (see preparation of 121) (300 mg) and 2-bromopropane (1.20 mL) in MeCN (3 mL) with potassium carbonate (192 mg) were heated at 60° C. in a sealed tube for 7 days. The reaction mixture was cooled down, diluted with DCM, washed with brine, dried (MgSO4) and the solvent removed in vacuo. The residue was purified using flash chromatography to yield 4-[isopropyl-(2-methoxy-ethyl)-amino]-piperidine-1-carboxylic acid tert-butyl ester as an oil (131 mg). Treatment of this compound with HCl in DCM/MeOH and basic wash with aqueous sodium bicarbonate yielded the desired amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946217B2
Source datasetuspto-grants-2015_02
ORD IDord-2cbc1c78d1ab45ff85ac153641fb9e2b
Source noteuspto-grants-2015_02