HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992525Generated: October 30, 2026
Sodium Hydroxide → HCID 10836335, compound
https://huagongshe.com/reaction/992525
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 10647511 | HCID 10647511 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10836335 | HCID 10836335 | — |
Reaction Steps
To a solution of 41.6 mg (0.091 mmol) ethyl2-fluoro4-[[(5,6-dihydro-5,5-dimethyl-8-(4-methylphenyl)-2-naphthalenyl)carbonyl]amino]-benzoate (Compound 40) in 2.0 ml EtOH and 2.0 ml of THF was added 40.0 mg NaOH (1.00 mmol, 1.0 ml of a 1 M aqueous solution). After stirring at room temperature for overnight, the reaction was quenched by the addition of 10% HCl. Extraction with EtOAc, and drying of the organic layers over MgSO4, provided a solid after removal of the solvent under reduced pressure. Crystallization from CH3CN afforded the title compound as a pale-yellow solid. 1H NMR (d6-acetone): δ9.84 (1H, s), 7.94-7.83 (3H, m), 7.64 (1H, dd, J=2.0 Hz), 7.53 (2H, d, J=8.1 Hz), 7.23 (4H, s), 6.04 (1H, t, J=4.7 Hz, 2.38 (2H, d, J=4.7 Hz), 2.36 (3H, s), 1.35 (6H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06469028B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-2e6981397bc6464199523376da4a52b7 |
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| Source note | uspto-grants-2002_10 |
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