HCID 86619885, Verbindung → 1,2,3,4-Tetrahydroisoquinoline-7-sulfonamide
Reaktionsgleichung
C([NH:5][S:6]([C:9]1[CH:18]=[C:17]2[C:12]([CH2:13][CH2:14][N:15](C(=O)C(F)(F)F)[CH2:16]2)=[CH:11][CH:10]=1)(=[O:8])=[O:7])(C)(C)C>C(O)(C(F)(F)F)=O>[CH2:16]1[C:17]2[C:12](=[CH:11][CH:10]=[C:9]([S:6]([NH2:5])(=[O:7])=[O:8])[CH:18]=2)[CH2:13][CH2:14][NH:15]1Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
N-(tert-Butyl)-2-(trifluoroacetyl)-1,2,3,4-tetrahydroisoquinoline-7-sulfonamide (the product from step i), 1.78 g) was dissolved in TFA and stirred at room temperature for 96 h. The reaction was reduced in vacuo and the residue purified by column chromatography on silica gel 50% EtOAc/50% iso-hexane to give the subtitle compound as a white solid. Yield: 0.65 g
Aufarbeitung
- customthe residue purified by column chromatography on silica gel 50% EtOAc/50% iso-hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-a7fad896c9ca49fda8546af760adff7a
- Quelldatensatz
- uspto-grants-2014_05
- Patentnummer
- US08722883B2
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