HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77389Generated: October 25, 2026
Water → 7-bromo-3-(3-chlorophenyl)-2-methylisoquinolin-1(2H)-one
https://huagongshe.com/reaction/77389
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Methyl-4-nitrobenzenesulfonate | HCID 22582 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7-bromo-3-(3-chlorophenyl)isoquinolin-1(2H)-one | HCID 69928893 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-bromo-3-(3-chlorophenyl)-2-methylisoquinolin-1(2H)-one | HCID 69928548 | 50.2% |
Reaction Steps
7-Bromo-3-(3-chlorophenyl)isoquinolin-1(2H)-one (Intermediate 23A) (0.1 g, 0.299 mmol) was dissolved in THF (4 mL), under an atmosphere of nitrogen. Sodium hydride (0.018 g, 0.448 mmol) was added and reaction stirred for 30 minutes. The reaction was then cooled using an ice bath and methyl 4-nitrobenzenesulfonate (0.065 g, 0.299 mmol) was added. The reaction was allowed to warm to room temperature and left to stir overnight. Water was added to the reaction mixture and extracted with EtOAC (×2). The organics were combined and washed with brine, dried (MgSO4) filtered and concentrated under reduced pressure. The mixture was purified on silica (25 g column on Isolera 4) eluting with 0-10% methanol in dichloromethane to afford 7-bromo-3-(3-chlorophenyl)-2-methylisoquinolin-1(2H)-one (51 mg, 0.15 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841289B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-d964deca7655450c9db475cc20959061 |
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| Source note | uspto-grants-2014_09 |
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