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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236850Generated: November 3, 2026

N,1-dimethylpyrrolidin-3-amine → HCID 86619600, compound

https://huagongshe.com/reaction/2236850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,1-dimethylpyrrolidin-3-amineHCID 2758520—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 86619598HCID 86619598—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 86619600HCID 86619600101.6%

Reaction Steps

To a suspension of tert-butyl [4-(4-formyl-piperidin-1-yl)-phenyl]carbamate (0.20 g, 0.66 mmol) in methanol (5 mL) is added N,N′-dimethyl-3-aminopyrrolidine (0.15 g, 1.3 mmol). The reaction mixture is stirred for 20 minutes and then a mixture of zinc chloride (53 mg) and sodium cyanoborohydride (50 mg) in methanol (2 mL) is added in a dropwise fashion. After stirring overnight at room temperature, the reaction mixture is diluted with water and extracted 3× with ethyl acetate. The combined extracts were washed once with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give tert-butyl [4-(4-{[methyl-(1-methyl-pyrrolidin-3-yl)-amino]-methyl}-piperidin-1-yl)-phenyl]-carbamate as a foam (0.27 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713994B2
Source datasetuspto-grants-2010_05
ORD IDord-71c25c38e91b4ae29904c65522c371a8
Source noteuspto-grants-2010_05