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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243798Generated: October 30, 2026

4-Amino-1-Boc-piperidine → HCID 21064718, compound

https://huagongshe.com/reaction/1243798

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
ReactantHCID 21928118HCID 21928118—
SolventDimethylformamideHCID 6228—
ProductHCID 21064718HCID 2106471836.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a sealed tube was added 4-oxiranylmethoxy-pyridine (80 mg, 0.529 mmol) in 4 mL of DMF, followed by the addition of 4-amino-1-N-boc-piperidine (148 mg, 0.739 mmol). The reaction mixture was stirred at 80° C. for 48 h. The reaction mixture was concentrated in vacuo. The residue was loaded to a flash chromatography column. The column was eluted with 0–5% 2M NH3 in MeOH/CH2Cl2. The product fractions were collected and concentrated to afford 68 mg (36.6%) of 4-[2-hydroxy-3-(pyridin-4-yloxy)-propylamino]-piperidine-1-carboxylic acid tert-butyl ester as a light brown oil. (TLC: Rf=0.15, 5% 2M NH3 in MeOH/CH2Cl2, UV). ES+ 352.43 m/z (MH+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119102B2
Source datasetuspto-grants-2006_10
ORD IDord-c1b06d15f4904a6da157b3918827507b
Source noteuspto-grants-2006_10