Hydrochloric Acid → 6-(5-Aminomethyl-4-chloro-pyridin-3-yl)-1-methyl-3,4-dihydro-1H-quinolin-2-one hydrochloride
Reaktionsgleichung
[Cl:1][C:2]1[C:7]([C:8]2[CH:9]=[C:10]3[C:15](=[CH:16][CH:17]=2)[N:14]([CH3:18])[C:13](=[O:19])[CH2:12][CH2:11]3)=[CH:6][N:5]=[CH:4][C:3]=1[CH2:20][NH:21][S@@](C(C)(C)C)=O.Cl>CO>[ClH:1].[NH2:21][CH2:20][C:3]1[C:2]([Cl:1])=[C:7]([C:8]2[CH:9]=[C:10]3[C:15](=[CH:16][CH:17]=2)[N:14]([CH3:18])[C:13](=[O:19])[CH2:12][CH2:11]3)[CH:6]=[N:5][CH:4]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
In analogy to the procedure described for the preparation of example 42, reaction of (R)-2-methyl-propane-2-sulfinic acid [4-chloro-5-(1-methyl-2-oxo-1,2,3,4-tetrahydro-quinolin-6-yl)-pyridin-3-ylmethyl]-amide (example 217) with hydrogen chloride (in dixoane) in methanol gave the title compound as a yellow solid. MS: 302.4 (M+H+).
Quellen und Nachweise
- ORD-Eintrag
- ord-767443bd5dea46e3a0f7513923cebd02
- Quelldatensatz
- uspto-grants-2016_02
- Patentnummer
- US09260408B2
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