HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247838Generated: November 1, 2026
Formic Acid → [5-amino-1-(2-hydroxyethyl)-1H-pyrazol-4-yl]formamide
https://huagongshe.com/reaction/1247838
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(4,5-Diamino-1H-pyrazol-1-YL)ethanol sulfate | HCID 87481667 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | [5-amino-1-(2-hydroxyethyl)-1H-pyrazol-4-yl]formamide | HCID 86593415 | — |
Reaction Steps
To a suspension of 2-(4,5-diamino-1H-pyrazol-1-yl)ethanol sulfate (5 g) in dichloromethane (50 ml) was added triethylamine (6.38 ml) at 0° C., and the mixture was stirred at 0° C. for 10 minutes. A mixture of acetic anhydride (2.16 ml) and formic acid (1.74 ml) was stirred at 40° C. for 30 minutes, cooled to 0° C. and added dropwise to the above solution at 0° C. The whole mixture was stirred at 0° C. for 2 hours. To the mixture was added brine, and the whole mixture was extracted with tetrahydrofuran. The extract was dried over magnesium sulfate and evaporated under reduced pressure to give crude [5-amino-1-(2-hydroxyethyl)-1H-pyrazol-4-yl]formamide, which was used in the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07129232B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-4ec120488a2948afb6a0e318d06e4578 |
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| Source note | uspto-grants-2006_10 |
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