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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374108Generated: October 30, 2026

Indazole-3-carboxylic acid → HCID 14999062, compound

https://huagongshe.com/reaction/374108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndazole-3-carboxylic acidHCID 78250—
ReactantHCID 14999061HCID 14999061—
SolventDimethylformamideHCID 6228—
ProductHCID 14999062HCID 1499906218.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 1H-indazole-3-carboxylic acid (2.2 g) in N,N-dimethylformamide (40 ml), N,N'-carbonyldiimidazole (2.2 g) is added, and the mixture is heated at 60° C. for 3.5 hours. A solution of 6-amino-1-benzyl-3,4-dimethylhexahydro-1H-1,4-diazepine (3.0 g) in N,N-dimethylformamide (10 ml) is added to the mixture, and the mixture is stirred at 25° C. for 2 hours. The solvent is evaporated under reduced pressure, and the residue is diluted with water and extracted with chloroform. The organic layer is washed successively with 10% aqueous sodium hydroxide solution, water and saturated aqueous sodium chloride solution, and dried over sodium sulfate. The solvent is evaporated under reduced pressure, and the residue is chromatographed on silica gel with elution 10% methanol-acetone. Fractions containing the title compound are pooled and evaporated under reduced pressure to give the title compound (0.9 g) which is one isomer with lower polarity in two isomers produced in the above reaction, m.p. 203°-205° C. (recrystallized from isopropyl alcohol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166341
Source datasetuspto-grants-1992_11
ORD IDord-d75a18d3bdd94d3282ac3c73567cf019
Source noteuspto-grants-1992_11