HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490091Generated: October 30, 2026
Water → 5-cyano-N-(4-methoxybenzyl)-3-methylindazole
https://huagongshe.com/reaction/490091
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 5-bromo-N-(4-methoxybenzyl)-3-methylindazole | HCID 69000908 | — |
| Catalyst | Nickel(II) bromide | HCID 278492 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 5-cyano-N-(4-methoxybenzyl)-3-methylindazole | HCID 68999208 | 99.4% |
Reaction Steps
To a solution of 5-bromo-N-(4-methoxybenzyl)-3-methylindazole 105 (0.12 g, 0.363 mmol) in NMP (N-methylpyrrolidinone; 2 mL) was added sodium cyanide (0.035 g, 0.714 mmol) and nickel bromide (0.079 g, 0.362 mmol). The reaction mixture was heated in a microwave reactor at 180° C. for 20 minutes. Ethyl acetate (100 mL) was added and the organic layer was washer with water and brine. The organic layer was dried over sodium sulfate. The organic solvent was evaporated under reduced pressure. The crude product was purified by flash column chromatography to yield the desired 5-cyano-N-(4-methoxybenzyl)-3-methylindazole 106 (0.1 g, 0.361 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07528132B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-a3228b1610b64aa3881d2ef461f1f1f5 |
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| Source note | uspto-grants-2009_05 |
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