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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Indazole-3-carboxylic acid | HCID 78250 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 10082174 | HCID 10082174 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10428804 | HCID 10428804 | 54.3% |
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
| 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-fea217bdc23f46d0a98aaa52d0692b3f |
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| Source note | uspto-grants-1992_11 |
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