Hydrochloric Acid → 2-[6-(3-Hydroxyazetidin-1-yl)pyrimidin-4-yl]-4-(1H-1,2,3-triazol-1-yl)-1,2-dihydro-3H-pyrazol-3-one hydrochloride
Reaktionsgleichung
[ClH:1].[OH:2][CH:3]1[CH2:6][N:5]([C:7]2[N:12]=[CH:11][N:10]=[C:9]([N:13]3[C:17](=[O:18])[C:16]([N:19]4[CH:23]=[CH:22][N:21]=[N:20]4)=[CH:15][NH:14]3)[CH:8]=2)[CH2:4]1>O1CCOCC1>[ClH:1].[OH:2][CH:3]1[CH2:4][N:5]([C:7]2[N:12]=[CH:11][N:10]=[C:9]([N:13]3[C:17](=[O:18])[C:16]([N:19]4[CH:23]=[CH:22][N:21]=[N:20]4)=[CH:15][NH:14]3)[CH:8]=2)[CH2:6]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
3 ml of a 4 N solution of hydrogen chloride in dioxane are added to 105 mg (0.4 mmol) of the compound from Example 88 and the mixture is stirred at RT for 1 h. The solid is filtered off, washed with tert-butyl methyl ether and dried under a high vacuum.
Aufarbeitung
- filtrationThe solid is filtered off
- washwashed with tert-butyl methyl ether
- customdried under a high vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-c02b98417a3c4432a34a0a59bc257220
- Quelldatensatz
- uspto-grants-2015_03
- Patentnummer
- US08987261B2
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