HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639644Generated: November 1, 2026
HCID 178499180, compound → HCID 178499176, compound
https://huagongshe.com/reaction/1639644
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178499180 | HCID 178499180 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178499176 | HCID 178499176 | 98.9% |
Reaction Steps
A suspension of 4-nitro-1H-pyrazole-3-carboxylic acid methyl ester (1.084 Kg, 6.33 mol, 1.0 wt) and ethanol (10.84 L, 10.0 vol) was heated to and maintained at 30 to 35° C. until complete dissolution occurred. 10% Palladium on carbon (10% Pd/C wet paste, 0.152 Kg, 0.14 wt) was charged to a separate flask under nitrogen and a vacuum/nitrogen purge cycle was performed three times. The solution of 4-nitro-1H-pyrazole-3-carboxylic acid methyl ester in ethanol was charged to the catalyst and a vacuum/nitrogen purge cycle was performed three times. A vacuum/hydrogen purge cycle was performed three times and the reaction was placed under an atmosphere of hydrogen. The reaction mixture was stirred at 28 to 30° C. until deemed complete by 1H NMR analysis (d6-DMSO). The mixture was filtered under nitrogen and concentrated under vacuum at 35 to 45° C. to give 4-amino-1H-pyrazole-3-carboxylic acid methyl ester (0.883 Kg, 98.9%) as a purple solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110573B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-d40a72c3cfe04ad79d1520d01bd8ae82 |
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| Source note | uspto-grants-2012_02 |
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