Reaktionsgleichung
B(O[O-])=O.[Na+].C(OC(=O)C)(=[O:8])C.CO.[CH3:15][O:16][C:17]1[CH:37]=[CH:36][C:20]2[NH:21][C:22]([S:24][CH2:25][C:26]3[C:31]([CH3:32])=[C:30]([O:33][CH3:34])[C:29]([CH3:35])=[CH:28][N:27]=3)=[N:23][C:19]=2[CH:18]=1>O.C1(C)C=CC=CC=1.CO>[CH3:15][O:16][C:17]1[CH:37]=[CH:36][C:20]2[NH:21][C:22]([S:24]([CH2:25][C:26]3[C:31]([CH3:32])=[C:30]([O:33][CH3:34])[C:29]([CH3:35])=[CH:28][N:27]=3)=[O:8])=[N:23][C:19]=2[CH:18]=1Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
Sodium perborate 4H2O (11.2 g, 73.0 mmol) was suspended in water (50 ml), followed by the dropwise addition of a solution of acetic anhydride (6.87 ml, 73.0 mmol)/methanol (5.75 ml) at 15.4° C. over 6 minutes and then, the mixture was stirred for about 13 min to prepare a homogenous solution (bulk temperature; 15.4° C. to 19.4° C.). The resulting solution was added dropwise to a solution (220 ml) of 5-methoxy-2-[(4-methoxy-3,5-dimethyl-2-pyridyl)methylthio]-1H-benzimidazole (20.0 g, 60.8 mmol) in toluene/methanol (10:1) at −20° C. over 2 hr. The resulting mixture was further stirred at the same temperature for 1 hr. The resulting crystals were collected by filtration, washed for three times with water (20 ml) and washed twice with tert-butyl methyl ether (20 ml). The resulting crystals were dried, to give the title compound (17.8 g, yield; 85.0%) as a white solid.
Aufarbeitung
- customto prepare a homogenous solution (bulk temperature; 15.4° C. to 19.4° C.)
- stirringThe resulting mixture was further stirred at the same temperature for 1 hr
- filtrationThe resulting crystals were collected by filtration
- washwashed for three times with water (20 ml)
- washwashed twice with tert-butyl methyl ether (20 ml)
- customThe resulting crystals were dried
Quellen und Nachweise
- ORD-Eintrag
- ord-58273e4b5fcc443098064e387c05d6c3
- Quelldatensatz
- uspto-grants-2001_11
- Patentnummer
- US06313303B1
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