1,4-Dioxane hydrochloride → [3-cyclopropyl-4-(4-fluorophenyl)-2,2-dimethyl-2H-chromen-7-yl]amine
Reaktionsgleichung
[CH:1]1([C:4]2[C:5]([CH3:30])([CH3:29])[O:6][C:7]3[C:12]([C:13]=2[C:14]2[CH:19]=[CH:18][C:17]([F:20])=[CH:16][CH:15]=2)=[CH:11][CH:10]=[C:9]([NH:21]C(=O)OC(C)(C)C)[CH:8]=3)[CH2:3][CH2:2]1.Cl.O1CCOCC1>>[CH:1]1([C:4]2[C:5]([CH3:30])([CH3:29])[O:6][C:7]3[C:12]([C:13]=2[C:14]2[CH:19]=[CH:18][C:17]([F:20])=[CH:16][CH:15]=2)=[CH:11][CH:10]=[C:9]([NH2:21])[CH:8]=3)[CH2:3][CH2:2]1Komponenten
3
Versuchsvorschrift
The compound obtained in (2) described above (115 mg) and 4N hydrochloric acid-dioxane solution (4 mL) were treated in the same manner as Reference Example 5(5) to give the titled compound as a crude product (a yellow powder).
Quellen und Nachweise
- ORD-Eintrag
- ord-21de8550d0944e9cbc46a5e4b24179cc
- Quelldatensatz
- uspto-grants-2013_04
- Patentnummer
- US08410166B2
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