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Sodium Bicarbonate → 7-Methanesulphonamido-1,2,4,5-tetrahydro-3H-3-benzazepine

HRID 329381
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 329381
C(OC([N:8]1[CH2:14][CH2:13][C:12]2[CH:15]=[CH:16][C:17]([NH:19][S:20]([CH3:23])(=[O:22])=[O:21])=[CH:18][C:11]=2[CH2:10][CH2:9]1)=O)(C)(C)C.C(=O)(O)[O-].[Na+]>C(O)=O>[CH3:23][S:20]([NH:19][C:17]1[CH:16]=[CH:15][C:12]2[CH2:13][CH2:14][NH:8][CH2:9][CH2:10][C:11]=2[CH:18]=1)(=[O:21])=[O:22]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 516892Sodium BicarbonateHCID 187652003-Tertiary-butoxycarbonyl-7-methanesulphonamido-1,2,4,5-tetrahydro-3H-3-benzazepine

Produkt 1

HCID 187651877-Methanesulphonamido-1,2,4,5-tetrahydro-3H-3-benzazepine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 284Formic AcidLösungsmittel

Versuchsvorschrift

3-Tertiary-butoxycarbonyl-7-methanesulphonamido-1,2,4,5-tetrahydro-3H-3-benzazepine (0.6 g) and 98% formic acid (10 ml) were stirred together at room temperature for 2 hours. The solvent was evaporated in vacuo to give an oil which was basified with aqueous sodium bicarbonate. The aqueous solution was evaporated in vacuo and the residue was triturated with hot isopropanol. The isopropanol was decanted and evaporated in vacuo to give a solid which was recrystallised from ethyl acetate/hexane to give the title compound, yield 0.22 g.

Aufarbeitung

  1. customThe solvent was evaporated in vacuo
  2. customto give an oil which
  3. customThe aqueous solution was evaporated in vacuo
  4. customthe residue was triturated with hot isopropanol
  5. customThe isopropanol was decanted
  6. customevaporated in vacuo
  7. customto give a solid which
  8. customwas recrystallised from ethyl acetate/hexane

Quellen und Nachweise

ORD-Eintrag
ord-909eaa2493114a61a056d45996e32ebe
Quelldatensatz
uspto-grants-1990_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04891372

Notizen zur Reaktion

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