Sodium Bicarbonate → 5-(Benzoxazol-2-yl)-2-methyl-1-neopentylbenzimidazole
Reaktionsgleichung
[CH2:1]([NH:6][C:7]1[CH:13]=[CH:12][C:11]([C:14]2[O:15][C:16]3[CH:22]=[CH:21][CH:20]=[CH:19][C:17]=3[N:18]=2)=[CH:10][C:8]=1[NH2:9])[C:2]([CH3:5])([CH3:4])[CH3:3].Cl.[C:24](=N)(OC)[CH3:25].C(=O)([O-])O.[Na+]>CO>[O:15]1[C:16]2[CH:22]=[CH:21][CH:20]=[CH:19][C:17]=2[N:18]=[C:14]1[C:11]1[CH:12]=[CH:13][C:7]2[N:6]([CH2:1][C:2]([CH3:5])([CH3:4])[CH3:3])[C:24]([CH3:25])=[N:9][C:8]=2[CH:10]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a methanol (5 mL) solution of 2-(2-neopentylaminoanilin-5-yl)benzoxazole (see Working Example 81-2) (192 mg, 0.650 mmol) was added methyl acetimidate hydrochloride (107 mg, 0.975 mmol), and this was heated to reflux for 2 hours. After the reaction was complete, saturated aqueous sodium hydrogen carbonate solution was added, and this was extracted with ethyl acetate. After the organic layer obtained was dried over anhydrous sodium sulfate, it was filtered and concentrated. The crystals obtained were purified by silica gel column chromatography to yield the title compound (155 mg, 75% yield) as white crystals.
Aufarbeitung
- temperaturethis was heated
- temperatureto reflux for 2 hours
- extractionthis was extracted with ethyl acetate
- customAfter the organic layer obtained
- dry with materialwas dried over anhydrous sodium sulfate, it
- filtrationwas filtered
- concentrationconcentrated
- customThe crystals obtained
- customwere purified by silica gel column chromatography
Quellen und Nachweise
- ORD-Eintrag
- ord-6afd0dc9d4274c34b7cb3c215efa26de
- Quelldatensatz
- uspto-grants-2014_09
- Patentnummer
- US08829035B2
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