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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Indazole-3-carboxylic acid | HCID 78250 | — |
| Reactant | HCID 14999061 | HCID 14999061 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14999062 | HCID 14999062 | 18.5% |
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
| 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-d75a18d3bdd94d3282ac3c73567cf019 |
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| Source note | uspto-grants-1992_11 |
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