Sodium Bicarbonate → 5-(Benzoxazol-2-yl)-1-(4-methoxycarbonylphenylmethyl)-2-methylbenzimidazole

HRID 74299Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 74299
[CH3:1][O:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([CH2:11][NH:12][C:13]2[CH:19]=[CH:18][C:17]([C:20]3[O:21][C:22]4[CH:28]=[CH:27][CH:26]=[CH:25][C:23]=4[N:24]=3)=[CH:16][C:14]=2[NH2:15])=[CH:7][CH:6]=1)=[O:4].Cl.[C:30](=N)(OC)[CH3:31].C(=O)([O-])O.[Na+]>CO>[O:21]1[C:22]2[CH:28]=[CH:27][CH:26]=[CH:25][C:23]=2[N:24]=[C:20]1[C:17]1[CH:18]=[CH:19][C:13]2[N:12]([CH2:11][C:8]3[CH:7]=[CH:6][C:5]([C:3]([O:2][CH3:1])=[O:4])=[CH:10][CH:9]=3)[C:30]([CH3:31])=[N:15][C:14]=2[CH:16]=1

Komponenten

5

Versuchsvorschrift

To a solution of 2-(2-(4-methoxycarbonylphenylmethyl)aminoanilin-5-yl)benzoxazole (see Working Example 113-2) (59.0 mg, 0.159 mmol) in methanol (3 mL) was added methyl acetimidate hydrochloride (19 mg, 0.174 mmol), and this was heated to reflux for 1.5 hours. After the reaction was complete, saturated aqueous sodium hydrogen carbonate solution was added, and this was stirred for several minutes at room temperature. The crystals obtained were filtered, and after being washed with water, they were dried to yield the title compound (62.2 mg, 98% yield) as yellow crystals.

Aufarbeitung

  1. temperaturethis was heated
  2. temperatureto reflux for 1.5 hours
  3. customThe crystals obtained
  4. filtrationwere filtered
  5. washafter being washed with water, they
  6. customwere dried

Quellen und Nachweise

ORD-Eintrag
ord-b7ff4d4c6580482bae322519dd1eab08
Quelldatensatz
uspto-grants-2014_09
Patentnummer
US08829035B2

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