HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470319Generated: October 30, 2026
HCID 59784645, compound → HCID 59785015, compound
https://huagongshe.com/reaction/470319
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 59784645 | HCID 59784645 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | HCID 59785015 | HCID 59785015 | 73.9% |
Reaction Steps
A suspension of 3-Amino-1-[4-(4-dimethylamino-phenyl)-pyrimidin-2-yl]-1H-pyrazole-4-carboxylic acid ethyl ester (250 mg, 0.71 mM) in 1 N KOH (3 ml) and MeOH (4 ml) was heated at 95° C. for 1 hr allowing some methanol to distil off. The reaction was cooled to room temperature and neutralized with 1 N HCl. The resulting precipitate was collected via filtration, washed with water (1×3 ml) and then dried in vacuo overnight to afford 3-Amino-1-[4-(4-dimethylamino-phenyl)-pyrimidin-2-yl]-1H-pyrazole-4-carboxylic acid (170 mg, 73% yield) as a yellow solid. ES-MS MH+325.4 1H NMR (300 MHz, ppm, DMSO-d6): 8.72 (s, 1H), 8.60 (d, 1H), 8.15 (d, 2H), 7.70 (d, 1H), 6.82 (d, 2H), 5.77 (br, 2H), 3.03 (s, 6H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08629147B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-ece18b268c074df4b1e70c8d75862be8 |
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| Source note | uspto-grants-2014_01 |
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