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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264431Generated: October 31, 2026

4-Amino-1-Boc-piperidine → HCID 68784496, compound

https://huagongshe.com/reaction/2264431

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
ReactantHCID 58972435HCID 58972435—
SolventDimethylformamideHCID 6228—
ProductHCID 68784496HCID 68784496—

Reaction Steps

A mixture of 2-chloro-5,5,7,7-tetramethyl-5,7-dihydro-furo[3,4-d]pyrimidine (1.60 g, 7.52 mmol, 1.0 equiv; intermediate B1) and 4-amino-piperidine-1-carboxylic acid tert-butyl ester (1.81 g, 9.03 mmol, 1.2 equiv; commercially available) in anhydrous DMF (6 mL) was heated by microwave irradiation to 150° C. for 30 min. The organic phase was concentrated under reduced pressure and the residue purified with column chromatography on silica eluting with a gradient of heptane/ethyl acetate (10:1)→ethyl acetate providing 1.26 g (45%) of the title compound. MS (ISP): 377.4 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855194B2
Source datasetuspto-grants-2010_12
ORD IDord-82a4df11d163402681e0da6700f57495
Source noteuspto-grants-2010_12