Diisopropylethylamine → HCID 58026360, Verbindung
Reaktionsgleichung
[Cl:1][C:2]1[C:11]([O:12][CH3:13])=[C:10]2[C:5]([CH:6]=[C:7]([C:14]([OH:16])=O)[N:8]=[CH:9]2)=[CH:4][CH:3]=1.[NH:17]1[CH:21]=[CH:20][N:19]=[C:18]1[NH:22][C:23]([C:25]1[C:33]2[NH:32][C:31]([NH2:34])=[N:30][C:29]=2[CH:28]=[CH:27][CH:26]=1)=[O:24].CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C>CN(C=O)C>[NH:19]1[CH:20]=[CH:21][N:17]=[C:18]1[NH:22][C:23]([C:25]1[C:33]2[N:32]=[C:31]([NH:34][C:14]([C:7]3[N:8]=[CH:9][C:10]4[C:5]([CH:6]=3)=[CH:4][CH:3]=[C:2]([Cl:1])[C:11]=4[O:12][CH3:13])=[O:16])[NH:30][C:29]=2[CH:28]=[CH:27][CH:26]=1)=[O:24]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
10 mg (13%) of 7-chloro-8-methoxy-isoquinoline-3-carboxylic acid [4-(1H-imidazol-2-ylcarbamoyl)-1H-benzoimidazol-2-yl]-amide was synthesized according to the general procedure A using 7-chloro-8-methoxy-isoquinoline-3-carboxylic acid (from previous step), 36.3 mg (0.15 mmol) of intermediate B (2-amino-3H-benzoimidazole-4-carboxylic acid (1H-imidazol-2-yl)-amide), 69 mg (0.18 mmol) of HBTU, 0.106 mL (0.6 mmol) of DIEA in 2 mL of DMF stirring at 80° C. for 2 h. LCMS: 462 (M+1)+.
Quellen und Nachweise
- ORD-Eintrag
- ord-77e5ee9f8f504fa8b6a17d0572ad96d6
- Quelldatensatz
- uspto-grants-2013_12
- Patentnummer
- US08598353B2
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