Sodium Hydroxide → 2-[4-(5-fluorobenzothiazol-2-yl]methyl-3,4-dihydro-3-oxo-2H-1,4-benzothiazin-2-yl]acetic acid

HRID 1655898Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1655898
[F:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][C:8]([CH2:10][N:11]3[C:16]4[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=4[S:14][CH:13]([CH2:21][C:22]([O:24]CC)=[O:23])[C:12]3=[O:27])=[N:7][C:6]=2[CH:28]=1.[OH-].[Na+]>>[F:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][C:8]([CH2:10][N:11]3[C:16]4[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=4[S:14][CH:13]([CH2:21][C:22]([OH:24])=[O:23])[C:12]3=[O:27])=[N:7][C:6]=2[CH:28]=1

Komponenten

3

Versuchsvorschrift

The compound of Example 1 (275 mg) was dissolved in methanol-dioxane (1:2, v/v, 3 ml), and 0.7 ml of 2N sodium hydroxide solution was added dropwise to the solution with stirring at room temperature. The mixture was stirred for further 90 minutes. The solvent was distilled off and the residue was diluted with water, then the aqueous mixture was acidified with 10% hydrochloric acid. The precipitated solid was crystallized from chloroform-hexane to give 196 mg of the title compound. The structural formula and physical data of this compound are shown in Table 25.

Aufarbeitung

  1. stirringThe mixture was stirred for further 90 minutes
  2. distillationThe solvent was distilled off
  3. additionthe residue was diluted with water
  4. customThe precipitated solid was crystallized from chloroform-hexane

Quellen und Nachweise

ORD-Eintrag
ord-be83ef69fa294685a6111271de31bf90
Quelldatensatz
uspto-grants-1993_10
Patentnummer
US05252571

Notizen zur Reaktion

Wird geladen…