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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374104Generated: October 30, 2026

Indazole-3-carboxylic acid → HCID 10428804, compound

https://huagongshe.com/reaction/374104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndazole-3-carboxylic acidHCID 78250—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 10082174HCID 10082174—
SolventDichloromethaneHCID 6344—
ProductHCID 10428804HCID 1042880454.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 6-amino-1-benzyl-4-methylhexahydro-1H-1,4-diazepine (1.0 g) in dichloromethane (20 ml), 1H-indazole-3-carboxylic acid (740 mg) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (877 mg) are added, and the resulting mixture is stirred at 25° C. for 2 hours. The reaction mixture is washed successively with water and 10% aqueous sodium hydroxide solution, and dried over magnesium sulfate. The solvent is evaporated under reduced pressure, and the residue is chromatographed on silica gel with elution of acetone. Fractions containing the title compound are pooled and evaporated under reduced pressure to give the title compound (0.9 g) as an oil. The free base thus obtained is converted to the hemifumarate of the title compound in a usual manner, m.p. 192°-194° C. (recrystallized from ethanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166341
Source datasetuspto-grants-1992_11
ORD IDord-fea217bdc23f46d0a98aaa52d0692b3f
Source noteuspto-grants-1992_11