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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236748Generated: October 29, 2026

tert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylate → HCID 178452237, compound

https://huagongshe.com/reaction/2236748

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylateHCID 11011301—
Reactant4-methoxymethylene-6-bromo-4H-isoquinoline-1,3-dioneHCID 68692764—
SolventDimethylformamideHCID 6228—
ProductHCID 178452237HCID 17845223742.5%

Reaction Steps

A N,N-dimethylformamide solution (2.2 mL) of 6-bromo-4-methoxymethylene-4H-isoquinoline-1,3-dione (280 mg, 0.99 mmol), and tert-butyl 4-(4-aminophenyl)piperazine-1-carboxylate (300 mg, 1.08 mmol) is heated at 90° C. for 0.5 h. After cooling in the refrigerator, the precipitate is collected, and washed with N,N-dimethylformamide and ether to give 222 mg (42%) of the title compound as a yellow solid. MS (ESI) m/z 527.529 (M+H)+1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713994B2
Source datasetuspto-grants-2010_05
ORD IDord-087ad7a7d7974768899471ab1460699f
Source noteuspto-grants-2010_05