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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643967Generated: November 2, 2026

1-Methyl-4-piperidone → HCID 66755114, compound

https://huagongshe.com/reaction/1643967

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-4-piperidoneHCID 74049—
Reactanttert-Butyl (3R)-3-(aminomethyl)pyrrolidine-1-carboxylateHCID 1515152—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66755114HCID 6675511499%

Reaction Steps

To a solution of (R)-3-(aminomethyl)-1-N-Boc-pyrrolidine (252 mg, 1.26 mmol) and 1-methyl-4-piperidone (0.16 mL, 1.38 mmol) in THF (10 mL) MP-(OAc)3BH resin (Argonaut; 2.33 mmol/g; 1.35 g, 3.15 mmol) was added and the reaction mixture was agitated at room temperature for 24 hours. Then, the reaction mixture was filtered and concentrated in vacuo to afford (R)-3-[(1-methyl-piperidin-4-ylamino)-methyl]-pyrrolidine-1-carboxylic acid tert-butyl ester (370 mg, 99%) as an orange oil. The product was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119676B2
Source datasetuspto-grants-2012_02
ORD IDord-352b04c18671464b9d165daaa5fb7454
Source noteuspto-grants-2012_02