HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428825Generated: November 2, 2026
Potassium Hydroxide → HCID 135860564, compound
https://huagongshe.com/reaction/1428825
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 136337161 | HCID 136337161 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 135860564 | HCID 135860564 | 86.2% |
Reaction Steps
A mixture of 1-[6-(naphthalen-1-yloxy)-4-oxo-3,4-dihydro-quinazolin-2-yl]-1H-pyrazole-4-carboxylic acid ethyl ester (0.42 g, 0.99 mmol), 1M aq. KOH (5.0 mL) and THF (5.0 mL) was stirred for 4 h. The mixture was concentrated to remove the THF and the aqueous residue was acidified to pH 2 with 1M aq. HCl. The resulting precipitate was collected by filtration to provide the titled compound (0.34 g, 86%). MS (ESI): mass calcd. for C22H14N4O4, 398.1; m/z found, 399.1 [M+H]+. 1H NMR (500 MHz, DMSO-d6): 12.99 (s, 1H), 12.86 (s, 1H), 8.94 (s, 1H), 8.24 (s, 1H), 8.06 (d, J=8.1 Hz, 1H), 8.02 (d, J=8.3 Hz, 1H), 7.87 (d, J=8.2 Hz, 1H), 7.78 (d, J=8.2 Hz, 1H), 7.71 (dd, J=8.9, 2.9 Hz, 1H), 7.62 (t, J=7.5 Hz, 1H), 7.60-7.54 (m, 2H), 7.38 (s, 1H), 7.24 (d, J=7.4 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08937078B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-4041c72f6eeb40848372630168958b9a |
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| Source note | uspto-grants-2015_01 |
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