Trifluoroacetic acid → 5-Bromo-6-cyclopropyl-3-iodopyridin-2-amine
Reaktionsgleichung
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([NH2:11])=[N:6][C:7]=1[CH:8]1[CH2:10][CH2:9]1.FC(F)(F)C(O)=O.[I:19]N1C(=O)CCC1=O>>[Br:1][C:2]1[CH:3]=[C:4]([I:19])[C:5]([NH2:11])=[N:6][C:7]=1[CH:8]1[CH2:9][CH2:10]1Komponenten
4
Versuchsvorschrift
A solution of 5-bromo-6-cyclopropylpyridin-2-amine (2.1 g, 9.81 mmol), trifluoroaceticacid (170 mg, 1.47 mmol), N-iodosuccinimide (2.2 g, 9.81 mmol) stirred at room temperature for 30 minutes. Reaction mass was quenched with water, basified with ammonium hydroxide solution. Solid separated was filtered and dried to get 3.3 g (100% yield) of titled compound. 1H NMR (CDCl3, 300 MHz): δ 7.85 (s, 1H), 4.80-4.65 (bs, 2H), 2.39-2.25 (m, 1H), 1.0-0.90 (m, 4H). MS: m/z=338.9 (M+1).
Aufarbeitung
- customReaction mass
- customwas quenched with water
- customSolid separated
- filtrationwas filtered
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-1964b8422f8c46aebd9ca5d09c80cde2
- Quelldatensatz
- uspto-grants-2016_05
- Patentnummer
- US09353107B2
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