8-methoxy-N-propyl-1,2,3,4-tetrahydronaphthalen-2-amine → HCID 67250622, Verbindung
Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:12]=1[CH2:11][CH:10]([NH:13][CH2:14][CH2:15][CH3:16])[CH2:9][CH2:8]2.[N:17]1[N:21]2[CH:22]=[CH:23][CH:24]=[CH:25][C:20]2=[C:19]([CH2:26][C:27](O)=O)[CH:18]=1>>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:12]=1[CH2:11][CH:10]([N:13]([CH2:14][CH2:15][CH3:16])[CH2:27][CH2:26][C:19]1[CH:18]=[N:17][N:21]3[CH:22]=[CH:23][CH:24]=[CH:25][C:20]=13)[CH2:9][CH2:8]2Komponenten
3
Versuchsvorschrift
Synthesis works according to the preparation of A4-1 or A4-4 when using N-(8-methoxytetralin-2-yl)-N-propylamine (A2-1: R=OMe) and 3-pyrazolo[1,5-a]pyridinyl acetic acid (A3-13: R=OMe, Cy=3-pyrazolo[1,5-a]pyridinyl) (synthesis according to literature: Gmeiner, P. Arch Pharm 1988, Vol 321, p 517) and subsequent reaction according to the synthesis of A5-1.
Aufarbeitung
- customSynthesis
- customworks according to the preparation of A4-1 or A4-4 when
- customaccording to the synthesis of A5-1
Quellen und Nachweise
- ORD-Eintrag
- ord-8b5d7eea8ebf4d51bdfa9b89b424b50a
- Quelldatensatz
- uspto-grants-2014_04
- Patentnummer
- US08691839B2
Notizen zur Reaktion
Wird geladen…