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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796768Generated: November 3, 2026

Chloroform → HCID 22180271, compound

https://huagongshe.com/reaction/1796768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantAzobisisobutyronitrileHCID 6547—
ReactantChlorosuccinimideHCID 31398—
Reactant7-(4-Tert-butoxycarbonyl-piperazin-1-yl)-3,4-dihydro-2H-isoquinolin-1-oneHCID 10735270—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 22180271HCID 2218027112.2%

Reaction Conditions

Temperature90 °C

Reaction Steps

The compound (6.63 g) prepared in step (a) of Example 125 was dissolved in carbon tetrachloride (200 ml). N-Chlorosuccinimide (3.47 g) and AIBN (0.66 g) were added to the solution, and the mixture was heated at 90° C. with stirring for one hr. The temperature of the reaction solution was returned to room temperature. Chloroform was then added to the reaction solution, and the mixture was washed with water, followed by drying over anhydrous MgSO4 The solvent was then removed by distillation under the reduced pressure. The residue was crudely purified by column chromatography on silica gel (ethyl acetate). The solvent was removed by distillation under the reduced pressure. Chloroform was added to the residue, and the precipitated crystal was collected by filtration (and washed with diethyl ether) to give 7-(4-tert-butoxycarbonyl-piperazin-1-yl)-8-chloro-3,4-dihydro-2H-isoquinolin-1-one (0.89 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030120B2
Source datasetuspto-grants-2006_04
ORD IDord-6bdc6926ebfe43cb9bbd5be2c29dcdf2
Source noteuspto-grants-2006_04