HCID 178452762, Verbindung → HCID 178461256, Verbindung
Reaktionsgleichung
[Cl:1][C:2]1[C:7]([NH:8][CH2:9][C@H:10]2[CH2:15][CH2:14][C@H:13]([CH3:16])[CH2:12][CH2:11]2)=[C:6]([NH:17]C(=O)OC(C)(C)C)[CH:5]=[C:4]([Cl:25])[N:3]=1>Cl.O1CCOCC1>[Cl:1][C:2]1[C:7]([NH:8][CH2:9][C@H:10]2[CH2:11][CH2:12][C@H:13]([CH3:16])[CH2:14][CH2:15]2)=[C:6]([NH2:17])[CH:5]=[C:4]([Cl:25])[N:3]=1Komponenten
3
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of tert-butyl (2,6-dichloro-3-(((trans-4-methylcyclohexyl)methyl)amino)pyridin-4-yl)carbamate (150 g, 0.386 mol) in HCl/1,4-dioxane (4 M, 3.0 L) was stirred at 45° C. for 15 h. The mixture was concentrated under reduced pressure to give crude 2,6-dichloro-N3-((trans-4-methylcyclohexyl)methyl)pyridine-3,4-diamine.
Aufarbeitung
- concentrationThe mixture was concentrated under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-0b33c32f523d4018b35b14d010600496
- Quelldatensatz
- uspto-grants-2015_02
- Patentnummer
- US08962611B2
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