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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063125Generated: November 2, 2026

4-Amino-1-Boc-piperidine → HCID 23401055, compound

https://huagongshe.com/reaction/1063125

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
Reactant4-(2,3-Epoxypropoxy)benzamideHCID 12238247—
SolventDimethylformamideHCID 6228—
ProductHCID 23401055HCID 2340105540.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

4-Oxiranylmethoxy-benzamide (76 mg, 0.393 mmol) was dissolved in 8 mL of dry DMF, followed by the addition of 4-amino-1-N-boc-piperidine (178 mg, 0.889 mmol). The reaction mixture was stirred at 80° C. for 48 h. The reaction mixture was concentrated and the residue was purified by flash chromatography eluting with 0-5% 2M NH3 in MeOH/CH2Cl2. The product fractions were collected and concentrated to afford 62 mg of 4-[3-(4-carbamoyl-phenoxy)-2-hydroxy-propylamino]-piperidine-1-carboxylic acid tert-butyl ester as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964956B2
Source datasetuspto-grants-2005_11
ORD IDord-aedb107b873c4b09b3e55cc474a23bdf
Source noteuspto-grants-2005_11