Lithium Hydroxide → 6-[(4-chlorophenyl)sulfanyl]-3-pyridinylamine
Reaktionsgleichung
Cl[C:2]1[N:7]=[CH:6][C:5]([N+:8]([O-])=O)=[CH:4][CH:3]=1.[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([SH:18])=[CH:14][CH:13]=1.[OH-].[Li+]>CN(C=O)C>[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([S:18][C:2]2[N:7]=[CH:6][C:5]([NH2:8])=[CH:4][CH:3]=2)=[CH:14][CH:13]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
6-Chloro-3-nitropyridine (54.5 grams), 4-chlorothiophenol (50.0 grams), and lithium hydroxide (12.5 grams) were mixed in about 500 ml. of DMF and stirred overnight (about 18 hours) at room temperature. The reaction mixture was poured into ice-water, filtered, and the separated product washed three times with water and air dried, yield, 100 grams.
Aufarbeitung
- filtrationfiltered
- washthe separated product washed three times with water and air
- customdried
- customyield
Quellen und Nachweise
- ORD-Eintrag
- ord-f815efe19f0e4996899da64acd82ac39
- Quelldatensatz
- uspto-grants-1981_04
- Patentnummer
- US04264605
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