Tert-Butylamine → 4-Chloro-N-propyl-1-butanesulfonamide
Reaktionsgleichung
[CH2:1]([NH2:4])[CH2:2][CH3:3].C(N)(C)(C)C.[Cl:10][CH2:11][CH2:12][CH2:13][CH2:14][S:15](Cl)(=[O:17])=[O:16]>>[Cl:10][CH2:11][CH2:12][CH2:13][CH2:14][S:15]([NH:4][CH2:1][CH2:2][CH3:3])(=[O:17])=[O:16]Komponenten
4
Versuchsvorschrift
This was prepared in an analogous manner to that disclosed for Intermediate 41, using n-propylamine (commercially available, for example, from Aldrich) instead of t-butylamine, and 4-chloro-1-butanesulfonyl chloride (prepared according to White, E. H.; Lim, H. M. J. Org. Chem. 52, 1987, 11, 2162-2166) instead of 3-chloropropane sulfonyl chloride. Yield 88%. LCMS RT=2.54 min, ES+ve m/z 214 (M+H)+.
Aufarbeitung
- customThis was prepared in an analogous manner to
Quellen und Nachweise
- ORD-Eintrag
- ord-72884ef13e5c46468453f79f2a95c53b
- Quelldatensatz
- uspto-grants-2011_02
- Patentnummer
- US07884114B2
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