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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269721Generated: October 29, 2026

Triethylamine → HCID 22933578, compound

https://huagongshe.com/reaction/1269721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsocaproic acidHCID 12587—
ReactantSodium HydroxideHCID 14798—
Reactant1H-Indazol-5-amineHCID 88012—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 178418300HCID 178418300—
SolventDimethylformamideHCID 6228—
ProductHCID 22933578HCID 2293357871.4%

Reaction Steps

To a solution of 5-aminoindazole (1.00 g, 7.51 mmol) in N,N-dimethylformamide (15 ml) were added 4-methylvaleric acid (960 mg, 8.26 mmol), 1-ethyl-3-(3′-dimethylaminopropyl)carbodiimide monohydrochloride (1.72 g, 9.01 mmol), hydroxybenzotriazole (1.12 g, 8.26 mmol) and triethylamine (1.7 ml, 12.0 mmol), and the resulting mixture was stirred overnight at room temperature. Then, the reaction solution was cooled to 0° C. and a 1N-aqueous sodium hydroxide solution was added thereto, followed by extraction with chloroform. The organic layer was washed with water and then a saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was dissolved in a mixture of diethyl ether and methanol, followed by adding thereto hexane. The solid precipitated was collected by filtration and dried under reduced pressure to obtain N-(1H-indazol-5-yl)-4-methylpentanamide (1.24 g, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199147B2
Source datasetuspto-grants-2007_04
ORD IDord-f7c2bd37db8d4314ac9996e4cc5da421
Source noteuspto-grants-2007_04