Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 7-(4-Tert-butoxycarbonyl-piperazin-1-yl)-3,4-dihydro-2H-isoquinolin-1-one | HCID 10735270 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 22180271 | HCID 22180271 | 12.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06777414B1 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-c0815b21bd1f4737b93fa5cfb830de8f |
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| Source note | uspto-grants-2004_08 |
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