Indole-3-Butyric Acid → 3-Indolyl-butyramide
Reaktionsgleichung
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[CH2:10][CH2:11][C:12]([NH2:14])=[O:13].N1C2C(=CC=CC=2)C(CCCC(O)=O)=[CH:16]1.C(N1C=CN=C1)(N1C=CN=C1)=O>>[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[CH:10]([CH3:16])[CH2:11][C:12]([NH2:14])=[O:13]Komponenten
4
Versuchsvorschrift
This compound was prepared in the manner described above for (18a), using 3-indolebutyric acid and 1,1'-carbonyldimidazole. A 96% yield was obtained as a off-white solid: mp 86-87° C.
Aufarbeitung
- customThis compound was prepared in the manner
- customA 96% yield was obtained as a off-white solid
Quellen und Nachweise
- ORD-Eintrag
- ord-249859463c734e24ac4a0f36d77fc5ed
- Quelldatensatz
- uspto-grants-2000_09
- Patentnummer
- US06121307
Notizen zur Reaktion
Wird geladen…