N-(6-(1-amino-2-(3,5-difluorophenyl)ethyl)-5-bromopyridin-2-yl)acetamide hydrochloride → (S)-1-(5-bromo-2-(methylthio)pyrimidin-4-yl)-2-(3,5-difluorophenyl)ethanamine hydrochloride
Reaktionsgleichung
[ClH:1].NC(C1N=C(NC(=O)C)C=CC=1Br)CC1C=C(F)C=C(F)C=1.[Br:24][C:25]1[C:26]([C@@H:33]([NH:43][S@](C(C)(C)C)=O)[CH2:34][C:35]2[CH:40]=[C:39]([F:41])[CH:38]=[C:37]([F:42])[CH:36]=2)=[N:27][C:28]([S:31][CH3:32])=[N:29][CH:30]=1>>[ClH:1].[Br:24][C:25]1[C:26]([C@@H:33]([NH2:43])[CH2:34][C:35]2[CH:40]=[C:39]([F:41])[CH:38]=[C:37]([F:42])[CH:36]=2)=[N:27][C:28]([S:31][CH3:32])=[N:29][CH:30]=1Komponenten
3
Edukt 2
Produkt 1
Versuchsvorschrift
The title compound (12A) was prepared according to the method presented for the synthesis of compound 1F of Example 1 utilizing 11D. MS (m/z) 362.13 [M+H]+.
Quellen und Nachweise
- ORD-Eintrag
- ord-88d1eb8d299b4382a9bb7c437494b11a
- Quelldatensatz
- uspto-grants-2015_06
- Patentnummer
- US09050344B2
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