1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → HCID 86603118, Verbindung
Reaktionsgleichung
[C:1]([C:5]1[CH:20]=[CH:19][C:8]([CH2:9][NH:10][CH2:11][CH2:12][C:13]2[CH:18]=[CH:17][N:16]=[CH:15][CH:14]=2)=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[Cl:21][C:22]1[CH:23]=[C:24]2[C:28](=[C:29]([C:31](O)=[O:32])[CH:30]=1)[NH:27][CH:26]=[CH:25]2.CCN=C=NCCCN(C)C.Cl>C(Cl)Cl>[C:1]([C:5]1[CH:20]=[CH:19][C:8]([CH2:9][N:10]([CH2:11][CH2:12][C:13]2[CH:18]=[CH:17][N:16]=[CH:15][CH:14]=2)[C:31]([C:29]2[CH:30]=[C:22]([Cl:21])[CH:23]=[C:24]3[C:28]=2[NH:27][CH:26]=[CH:25]3)=[O:32])=[CH:7][CH:6]=1)([CH3:4])([CH3:2])[CH3:3]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
268 mg (1 mmol) of (4-tert-butyl-benzyl)-(2-pyridin-4-yl-ethyl)-amine, 196 mg (1 mmol) of 5-chloro-1H-indole-7-carboxylic acid and 217 mg (1.1 mmol) of EDC.HCl were stirred over night at rt in 20 ml DCM. The product was purified by column chromatography (silica gel; EtOAc) to yield 210 mg (47%) product as a colorless oil. MS (ISP) 446.0 (M+H)+.
Aufarbeitung
- customThe product was purified by column chromatography (silica gel; EtOAc)
Quellen und Nachweise
- ORD-Eintrag
- ord-72dd88f826bc4db481b093344c5edebe
- Quelldatensatz
- uspto-grants-2007_08
- Patentnummer
- US07259183B2
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