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

HRID 1655898ノート

反応式

HRID 1655898 の反応式
[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

参加物

3

反応物 2

HCID 14798Sodium HydroxideHCID 9909828Ethyl 2-[4-(5-fluorobenzothiazol-2-yl)methyl-3,4-dihydro-3-oxo-2H-1,4-benzothiazin-2-yl]acetate

生成物 1

HCID 117409862-[4-(5-fluorobenzothiazol-2-yl]methyl-3,4-dihydro-3-oxo-2H-1,4-benzothiazin-2-yl]acetic acid収率 76.4%

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-be83ef69fa294685a6111271de31bf90
出典データセット
uspto-grants-1993_10
特許番号
US05252571

反応ノート

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