HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497363Generated: November 2, 2026
Sodium hydride → 1-[(5-bromo-3-methyl-2H-indazol-2-yl)methyl]cyclopropanecarbonitrile
https://huagongshe.com/reaction/1497363
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | (1-Cyanocyclopropyl)methyl 4-methylbenzenesulfonate | HCID 22028201 | — |
| Reactant | HCID 178434225 | HCID 178434225 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[(5-bromo-3-methyl-2H-indazol-2-yl)methyl]cyclopropanecarbonitrile | HCID 117798613 | 12.4% |
Reaction Steps
To a suspension of 60% sodium hydride (143 mg) in N,N-dimethylformamide (3 ml) was added a solution of 5-bromo-3-methyl-1H-indazole (500 mg) in N,N-dimethylformamide (1 ml) at 0° C., and the mixture was stirred at the same temperature for 30 min. To the obtained reaction mixture was added (1-cyanocyclopropyl)methyl 4-methylbenzenesulfonate (420 mg), and the mixture was stirred at room temperature for 16 hr. To the reaction mixture was added saturated aqueous ammonium chloride solution, and the mixture was extracted with dichloromethane. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (60 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09199963B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-28d74b7291524c9aaa15b46ccdbdca5f |
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| Source note | uspto-grants-2015_12 |
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