HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410144Generated: October 25, 2026
Hydrochloric Acid → 5-amino-1-(4-methoxyphenyl)-3-methyl-1H-pyrazole-4-carbonitrile
https://huagongshe.com/reaction/1410144
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | (4-Methoxyphenyl)hydrazine | HCID 77023 | — |
| Reactant | (1-Ethoxyethylidene)malononitrile | HCID 79450 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-amino-1-(4-methoxyphenyl)-3-methyl-1H-pyrazole-4-carbonitrile | HCID 67120041 | 90.8% |
Reaction Steps
To a stirred solution of 2-(1-ethoxyethylidene) malononitrile (1.00 g, 6.66 mmol) in EtOH (8 mL) was added (4-methoxyphenyl)hydrazine (1.29 g, 9.32 mmol). (Prior to use the hydrazine its HCl salt was washed with NaHCO3/CH2Cl2. The organic phase was concentrated and used directly.) The solution was heated to 105° C. in the microwave for 20 min. CH2Cl2, was added and the organic phase was washed with 1M HCl and the organic extract was washed with aqueous NaHCO3. The solution was dried using a phase separator and concentrated under reduced pressure to give 5-amino-1-(4-methoxyphenyl)-3-methyl-1H-pyrazole-4-carbonitrile (1.38 g, 85%) which was used as such in the next step. The procedure was adapted from J. Med. Chem. 2004, 47, 5894-5911.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921402B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-c8d979d0b093445d8e7c674798bc169a |
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| Source note | uspto-grants-2014_12 |
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