Acetic Acid → 3'-(4-Fluorophenyl)-4-[2-(1,3,5-triethyl-1H-pyrazol-4-yl)-ethyl]-3,4,5,6-tetrahydro-2H-[1,2']bipyrazine hydrochloride
Reaktionsgleichung
[CH2:1]([N:3]1[C:7]([CH2:8][CH3:9])=[C:6]([CH2:10][CH:11]=O)[C:5]([CH2:13][CH3:14])=[N:4]1)[CH3:2].[F:15][C:16]1[CH:21]=[CH:20][C:19]([C:22]2[C:23]([N:28]3[CH2:33][CH2:32][NH:31][CH2:30][CH2:29]3)=[N:24][CH:25]=[CH:26][N:27]=2)=[CH:18][CH:17]=1.C(O)(=O)C.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(Cl)[Cl:53]>>[ClH:53].[F:15][C:16]1[CH:21]=[CH:20][C:19]([C:22]2[C:23]([N:28]3[CH2:29][CH2:30][N:31]([CH2:11][CH2:10][C:6]4[C:5]([CH2:13][CH3:14])=[N:4][N:3]([CH2:1][CH3:2])[C:7]=4[CH2:8][CH3:9])[CH2:32][CH2:33]3)=[N:24][CH:25]=[CH:26][N:27]=2)=[CH:18][CH:17]=1Komponenten
6
Edukt 5
Produkt 1
Versuchsvorschrift
Combine (1,3,5-triethyl-1H-pyrazol-4-yl)-acetaldehyde (0.16 g, 0.82 mmol) and 3′-(4-fluoro-phenyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl (0.24 g, 0.91 mmol) in DCM (10 mL) and stir at room temperature for 15 min. Then add glacial acetic acid (0.07 mL, 1.23 mmol) and sodium triacetoxyborohydride (0.26 g, 1.23 mmol) and stir for 3 hr. at room temperature. Purify using SCX chromatography and further purify using silica gel chromatography (5% 7 M ammonia in methanol/DCM). Dissolve the free base in methanol (5 mL) and treat with ammonium chloride (0.037 g). Concentrate the resulting solution to give the title compound (0.032 g, 83%). MS: m/z=437.3[M+H]+.
Aufarbeitung
- customat room temperature
- customPurify
- customfurther purify
- dissolutionDissolve the free base in methanol (5 mL)
- additiontreat with ammonium chloride (0.037 g)
- concentrationConcentrate the resulting solution
Quellen und Nachweise
- ORD-Eintrag
- ord-2e89aca8de5c43a093a6d2d04bea5ce2
- Quelldatensatz
- uspto-grants-2012_06
- Patentnummer
- US08202873B2
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