Hydrochloric Acid → HCID 178522041, compound

HRID 1803498Notes

Reaction equation

[F:1][C:2]([F:25])([F:24])[C:3]1[CH:4]=[C:5]([NH:9][C:10]([C:12]2[CH:13]=[C:14]3[C:19](=[CH:20][CH:21]=2)[C:18](Cl)=[N:17][N:16]=[C:15]3[Cl:23])=[O:11])[CH:6]=[CH:7][CH:8]=1.[OH-].[Na+].[O:28]1CCOCC1.Cl>O>[F:1][C:2]([F:25])([F:24])[C:3]1[CH:4]=[C:5]([NH:9][C:10]([C:12]2[CH:13]=[C:14]3[C:19](=[CH:20][CH:21]=2)[C:18]([OH:28])=[N:17][N:16]=[C:15]3[Cl:23])=[O:11])[CH:6]=[CH:7][CH:8]=1

Participants

Conditions

Temperature: 45 °C

Procedure

A mixture of 1,4-dichloro-phthalazine-6-carboxylic acid (3-trifluoromethyl-phenyl)-amide (0.304 mg, 0.787 mmol), 2N NaOH (4 mL, 8.00 mmol) and dioxane (6 mL) was stirred at 45° C. for 6 h. The reaction mixture was diluted with water, acidified with conc. HCl to ˜pH 4 and extracted with EtOAc (×3). The combined organic phase was washed with brine, dried (Na2SO4) and concentrated to afforded 4-chloro-1-hydroxy-phthalazine-6-carboxylic acid (3-trifluoromethyl-phenyl)-amide (0.112 g) as a white solid, 1H NMR (600 MHz, CDCl3) δ: 7.33 (d, 1H), 7.43 (t, 1H), 8.03 (s, 1H), 8.06 (d, 1H), 8.36 (dd, 1H), 8.42 (d, 1H), 8.56 (s, 1H), 10.28 (s, 1H), 11.9 (s, 1H) ppm, 1H NMR (500 MHz, d6-DMSO) δ: 7.52 (d, 1H), 7.65 (t, 1H), 8.08 (d, 1H), 8.26 (s, 1H), 8.43 (d, 1H), 8.47 (dd, 1H), 8.52 (s, 1H), 11.02 (s, 1H), 13.02 (s, 1H) ppm. m/z 368.13; and 1-chloro-4-hydroxy-phthalazine-6-carboxylic acid (3-trifluoromethyl-phenyl)-amide (0.083 g) as a white solid, 1H NMR (500 MHz, CDCl3) δ: 7.21 (d, 1H), 7.32 (t, 1H), 7.92 (d, 1H), 7.97 (d, 1H), 8.00 (s, 1H), 8.38 (d, 1H), 8.93 (s, 1H), 10.42 (s, 1H), 12.20 (s, 1H) ppm. m/z 368.13.

Workup

extractionextracted with EtOAc (×3)
washThe combined organic phase was washed with brine
dry with materialdried (Na2SO4)
concentrationconcentrated

Sources & evidence

ORD record: ord-b114b2b44bc24c40b4698916bbfd2a30
Source dataset: uspto-grants-2013_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08349836B2

Reaction notes

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