HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374102Generated: October 30, 2026
Indazole-3-carboxylic acid → HCID 14999040, compound
https://huagongshe.com/reaction/374102
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Indazole-3-carboxylic acid | HCID 78250 | — |
| Reactant | HCID 14999038 | HCID 14999038 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14999040 | HCID 14999040 | 67.4% |
Reaction Steps
To a solution of 1H-indazole-3-carboxylic acid (1.0 g) in N,N-dimethylformamide (20 ml), N,N'-carbonyldiimidazole (1.1 g) is added, and the mixture is heated at 60° C. for 2 hours. 6-Amino-1-(2,5-dimethylbenzyl)-4-methylhexahydro-1H-1,4-diazepine (1.5 g) is added to the reaction mixture, and the mixture is heated at 60° 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 water and aqueous sodium hydroxide solution, and dried over sodium 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 (1.6 g) as an oil. The free base thus obtained is converted to the fumarate of the title compound in a usual manner, m.p. 168°-170° C. (recrystallized from ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05166341 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-d9ae757b9b584b3d9a395e4113ddcc04 |
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| Source note | uspto-grants-1992_11 |
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