Sodium Hydroxide → HCID 59797443, Verbindung
Reaktionsgleichung
C[O:2][C:3](=[O:33])[CH2:4][O:5][C:6]1[C:19]2[S:18][C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[S:11][C:10]=2[C:9]([C:20]2[O:21][C:22]([N:27]3[CH2:32][CH2:31][O:30][CH2:29][CH2:28]3)=[CH:23][C:24](=[O:26])[CH:25]=2)=[CH:8][CH:7]=1.[OH-].[Na+:35]>CO>[Na+:35].[N:27]1([C:22]2[O:21][C:20]([C:9]3[C:10]4[S:11][C:12]5[C:17](=[CH:16][CH:15]=[CH:14][CH:13]=5)[S:18][C:19]=4[C:6]([O:5][CH2:4][C:3]([O-:33])=[O:2])=[CH:7][CH:8]=3)=[CH:25][C:24](=[O:26])[CH:23]=2)[CH2:32][CH2:31][O:30][CH2:29][CH2:28]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of [4-(6-Morpholin-4-yl-4-oxo-4H-pyran-2-yl)-thianthren-1-yloxy]-acetic acid methyl ester (1.41 g, 2.91 mmol) in anhydrous methanol (10 ml) was added sodium hydroxide (120 mg, 2.91 mmol) in a single portion. The solution was then stirred at room temperature for 24 hours whereupon the solvent was removed in vacuo to give the title compound as an off white paste (1.43 g, 98%) that required no further purification. m/z (LC-MS, ESP): RT=3.79 min, (M−−23)=468
Aufarbeitung
- customwas removed in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-e52a91aebc534d4dacbd50f3f2e5e93f
- Quelldatensatz
- uspto-grants-2008_09
- Patentnummer
- US07429660B2
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