HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241376Generated: November 1, 2026
2-(4-Fluorophenyl)-3-oxo-2,3-dihydropyridazine-4-carboxylic acid → HCID 59304368, compound
https://huagongshe.com/reaction/2241376
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(4-Fluorophenyl)-3-oxo-2,3-dihydropyridazine-4-carboxylic acid | HCID 66767171 | — |
| Reactant | HCID 68515968 | HCID 68515968 | — |
| Product | HCID 59304368 | HCID 59304368 | 55% |
Reaction Steps
Prepared by a 2-step process from 2-(4-(4-(4-amino-2-fluorophenoxy)-1-(4-methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-3-ylamino)piperidin-1-yl)ethanol (prepared as described in Example 101, Step A except using 2-(4-aminopiperidin-1-yl)ethanol) and 2-(4-fluorophenyl)-3-oxo-2,3-dihydropyridazine-4-carboxylic acid according to the procedure of Example 101, Step B. The crude material was rinsed with Et2O to afford 11 mg (55%) of the desired product. LRMS (ESI pos) m/e 603.1 (M+1). 1H-NMR (400 MHz, CD3OD/CDCl3) δ 8.42 (d, 1H), 8.31 (d, 1H), 8.13 (d, 1H), 8.0 (dd, 1H), 7.63 (m, 2H), 7.45 (d, 1H), 7.33 (t, 1H), 7.28 (t, 2H), 6.10 (d, 1H), 3.72 (m, 3H), 3.03 (m, 2H), 2.65 (m, 2H), 2.40 (m, 2H), 2.25 (m, 2H), 1.67 (m, 2H); 19F NMR (376 MHz, CD3OD/CDCl3) δ −112.1, −126.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07723330B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-57bb4e153e32446b9bc24c922d27f8ed |
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| Source note | uspto-grants-2010_05 |
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