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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantLithium borohydrideHCID 4148881—
Reactantmethyl 4-[(1H-indazol-5-ylcarbonyl)amino]cyclohexanecarboxylateHCID 18447321—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-hydroxymethylcyclohexyl)-1H-indazole-5-carboxamideHCID 2293401991%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199147B2
Source datasetuspto-grants-2007_04
ORD IDord-d6d891b5902e46d88a6533d3ea243c93
Source noteuspto-grants-2007_04