Water → 4-Fluorobenzoic acid 2-[6-(trifluoromethyl)-2-pyridinyl]hydrazide
Reaktionsgleichung
[F:1][C:2]([F:12])([F:11])[C:3]1[N:8]=[C:7]([NH:9][NH2:10])[CH:6]=[CH:5][CH:4]=1.[F:13][C:14]1[CH:22]=[CH:21][C:17]([C:18](Cl)=[O:19])=[CH:16][CH:15]=1.C(N(C(C)C)CC)(C)C.O>C1COCC1>[F:12][C:2]([F:1])([F:11])[C:3]1[N:8]=[C:7]([NH:9][NH:10][C:18](=[O:19])[C:17]2[CH:21]=[CH:22][C:14]([F:13])=[CH:15][CH:16]=2)[CH:6]=[CH:5][CH:4]=1Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a stirred solution of 6-(trifluoromethyl)pyridin-2-ylhydrazine (3.00 g, 16.4 mmol) and 4-fluorobenzoyl chloride (2.95 g, 18.63 mmol) in anhydrous THF (20 mL) at 0° C. under N2 was added diisopropylethylamine (2.41 g, 18.63 mmol). After 15 min, the solution was allowed to warm to room temperature over 1 h. Water (80 mL) was added, and the aqueous layer was extracted with ethyl acetate (2×100 mL). The organic extracts were combined, washed with water (100 mL), dried over MgSO4, and concentrated in vacuo to a tan solid. Recrystallization from ethyl acetate afforded the title compound of Step A as a white solid (3.16 g). 1H NMR (Me2SO-d6, 400 MHz) δ10.55 (s,1H), 9.10 (s, 1H), 8.00 (m,2H), 7.80 (t, 1H), 7.40 (t,2H), 7.15 (d, 1H), 6.90 (d, 1H).
Aufarbeitung
- extractionthe aqueous layer was extracted with ethyl acetate (2×100 mL)
- washwashed with water (100 mL)
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo to a tan solid
- customRecrystallization from ethyl acetate
Quellen und Nachweise
- ORD-Eintrag
- ord-a58c2e91749645178b984b5afd229705
- Quelldatensatz
- uspto-grants-1998_04
- Patentnummer
- US05739326
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