HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842715Generated: October 31, 2026
1H-Indazole-5-carbonitrile → 5-(Aminomethyl)-1H-indazole
https://huagongshe.com/reaction/842715
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1H-Indazole-5-carbonitrile | HCID 11126384 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(Aminomethyl)-1H-indazole | HCID 12096223 | — |
Reaction Steps
To a solution-of LiAlH4 (0.76 g, 20.1 mmol) in THF (10 mL) cooled to 0° C. was added a solution of 5-cyanoindazole (0.64 g, 4.47 mmol) in THF (10 mL) dropwise. After 0.5 h the reaction mixture was warmed to reflux for 2 h, then cooled to 0° C. and quenched by the careful addition of water (0.76 mL), 1.0 N sodium hydroxide (0.76 mL), and water (2.28 mL). This mixture was filtered through a pad of celite and washed with THF/MeOH (3:1, 300 mL). Removal of the solvent in vacuo provided a solid which was purified via flash column chromatography (25×150 mm column; elution with MeOH:CH2Cl2:CH2Cl2 saturated with NH3, 10:60:30). This afforded the title compound as a light yellow solid:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06376499B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-3b570a94bafb476f9cabe83f65de6e29 |
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| Source note | uspto-grants-2002_04 |
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