HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269759Generated: November 1, 2026
Sodium Hydroxide → N-(4-hydroxymethylcyclohexyl)-1H-indazole-5-carboxamide
https://huagongshe.com/reaction/1269759
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | methyl 4-[(1H-indazol-5-ylcarbonyl)amino]cyclohexanecarboxylate | HCID 18447321 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-hydroxymethylcyclohexyl)-1H-indazole-5-carboxamide | HCID 22934019 | 91% |
Reaction Steps
Lithium borohydride (10.0 mg, 0.459 mmol) was added to a solution of the methyl 4-[(1H-indazol-5-ylcarbonyl)amino]cyclohexanecarboxylate (30.0 mg, 0.0951 mmol) obtained in Example 186 in tetrahydrofuran (3.0 ml) at room temperature, and the resulting mixture was stirred for 2 hours with heating under reflux while maintaining the temperature. A 1N aqueous sodium hydroxide solution (0.8 ml) was added to the reaction solution, and the resulting mixture was stirred while being maintained at room temperature, and then was concentrated to dryness. The resulting crude product residue was stirred in methanol (3.0 ml) for another 1 hour with heating under reflux while maintaining the temperature. The resulting mixture was concentrated to dryness and purified by a silica gel column chromatography (eluent: chloroform/methanol=20/1) to obtain N-(4-hydroxymethylcyclohexyl)-1H-indazole-5-carboxamide (23.5 mg, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07199147B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-d6d891b5902e46d88a6533d3ea243c93 |
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| Source note | uspto-grants-2007_04 |
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