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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097978Generated: November 1, 2026

4-Amino-1-Boc-piperidine → 1,1-Dimethylethyl 4-(7-cyano-1,3-dihydro-1-oxo-2H-isoindol-2-yl)-1-piperidinecarboxylate

https://huagongshe.com/reaction/1097978

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
ReactantHCID 66812920HCID 66812920—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product1,1-Dimethylethyl 4-(7-cyano-1,3-dihydro-1-oxo-2H-isoindol-2-yl)-1-piperidinecarboxylateHCID 66812615—

Reaction Steps

To a solution of EXAMPLE 6C (300 mg) in tetrahydrofuran (2 mL) and N,N′-dimethylformamide (2 mL) was added tert-butyl 4-aminopiperidine-1-carboxylate (320 mg,) in N,N′-dimethylformamide (2 mL) and tetrahydrofuran (2 mL) at −40° C. The solution was warmed to ambient temperature over 2 hours, and stirred for 16 hours. The solvent was removed, and the concentrate was partitioned between ethyl acetate and water. The extract was washed with brine and concentrated, and the concentrate was purified by flash chromatography on silica gel with 80% ethyl acetate in hexanes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143284B2
Source datasetuspto-grants-2012_03
ORD IDord-d66f2dfb232349c19618d4d8d792bef2
Source noteuspto-grants-2012_03