Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 22144493 | HCID 22144493 | — |
| Reactant | HCID 69438029 | HCID 69438029 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22144532 | HCID 22144532 | — |
| Product | HCID 69439754 | HCID 69439754 | — |
Reaction Steps
1H-Indazole-5-carbonitrile hydrochloride (1.5 g) was suspended in ethanol (15 mL) at 0° C. The mixture was saturated with hydrogen chloride while the temperature was raised to room temperature. The reaction was then left overnight. Diethylether was added and the resulting precipitate, 1H-indazole-5-carboximidic acid ethyl ester.2HCl (1.39 g), was collected and dried in under high vacuum. According to synthetic method B except that pyridine (540 ?L) was added, from 4-amino-benzene-1,3-diol hydrochloride (0.36 mg) and 1H-indazole-5-carboximidic acid ethyl ester hydrochloride (0.71 g) was obtained the title compound (0.34 mg) as an off-white solid. The work-up of the reaction was modified as follows: After completion of the reaction, the mixture was diluted with ether and water, and filtered. The solids were washed with water and ether, and dried under high vacuum. MS: 252.4 (MH+); HPLC tR: 1.80 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07045539B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-836ab09b49b2446698ce988653caef7e |
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| Source note | uspto-grants-2006_05 |
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