HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098235Generated: November 1, 2026
2-(Ethoxymethylene)propanedinitrile → 5-amino-1-(2,3-dichlorophenyl)-1H-pyrazole-4-carbonitrile
https://huagongshe.com/reaction/1098235
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Ethoxymethylene)propanedinitrile | HCID 67152 | — |
| Reactant | (2,3-Dichlorophenyl)hydrazine | HCID 600691 | — |
| Reactant | 2,3-Dichlorophenylhydrazine HCl | HCID 12276572 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-amino-1-(2,3-dichlorophenyl)-1H-pyrazole-4-carbonitrile | HCID 2797250 | 100% |
Reaction Steps
(2,3-Dichlorophenyl)hydrazine hydrochloride (CAS no. 21938-47-6) (6.06 g, 28.4 mmol) was partitioned between EtOAc and 2M NaOH. Separated. The organic solution was dried (MgSO4), filtered and reduced to give the free base. 2-(Ethoxymethylene)malononitrile (3.47 g, 28.39 mmol) was added portionwise to a stirred solution of (2,3-dichlorophenyl)hydrazine in MeOH (50 mL), under nitrogen at 5° C. The resulting solution was allowed to stir for a further 1 hour. The reaction mixture was then heated to reflux and was stirred for 3 hours. The reaction mixture was allowed to cool to ambient temperature, then was evaporated to afford the product (7.19 g, 100%) which was used without further purification. 1H NMR (400 MHz, DMSO) δ 6.75 (2H, s), 7.48-7.53 (2H, m), 7.77 (1H, s), 7.79-7.84 (1H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143263B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-5d164f5faced4fa98ede5f335c4876e9 |
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| Source note | uspto-grants-2012_03 |
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