p-Acetamidobenzoic acid → HCID 22063359, Verbindung
Reaktionsgleichung
[NH2:1][C:2]1([C:8]#[N:9])[CH2:7][CH2:6][O:5][CH2:4][CH2:3]1.[CH3:10][C:11]([CH2:14][C@H:15]([NH2:19])[C:16]([OH:18])=O)([CH3:13])[CH3:12].[C:20]([NH:23][C:24]1[CH:32]=[CH:31][C:27]([C:28](O)=[O:29])=[CH:26][CH:25]=1)(=[O:22])[CH3:21]>>[C:20]([NH:23][C:24]1[CH:32]=[CH:31][C:27]([C:28]([NH:19][CH:15]([C:16](=[O:18])[NH:1][C:2]2([C:8]#[N:9])[CH2:7][CH2:6][O:5][CH2:4][CH2:3]2)[CH2:14][C:11]([CH3:10])([CH3:12])[CH3:13])=[O:29])=[CH:26][CH:25]=1)(=[O:22])[CH3:21]Komponenten
4
Versuchsvorschrift
The title compound was prepared from 4-amino-4-cyano-tetrahydropyran, L-neopentyl glycine and 4-acetylaminobenzoic acid analogous to the procedure described in Example 24.
Quellen und Nachweise
- ORD-Eintrag
- ord-7683be90518b4cac8f99332c4204c5b0
- Quelldatensatz
- uspto-grants-2007_09
- Patentnummer
- US07265132B2
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