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Lithium Hydroxide → [3-(4-Benzenesulfonylthiazol-5-ylmethyl)-5-fluoro-2-methylindol-1-yl]acetic acid

HRID 1944483
ノート
印刷プレビュー

反応式

HRID 1944483 の反応式
[OH-].[Li+].O1CCCC1.C[O:9][C:10](=[O:38])[CH2:11][N:12]1[C:20]2[C:15](=[CH:16][C:17]([F:21])=[CH:18][CH:19]=2)[C:14]([CH2:22][C:23]2[S:27][CH:26]=[N:25][C:24]=2[S:28]([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)(=[O:30])=[O:29])=[C:13]1[CH3:37]>O>[C:31]1([S:28]([C:24]2[N:25]=[CH:26][S:27][C:23]=2[CH2:22][C:14]2[C:15]3[C:20](=[CH:19][CH:18]=[C:17]([F:21])[CH:16]=3)[N:12]([CH2:11][C:10]([OH:38])=[O:9])[C:13]=2[CH3:37])(=[O:29])=[O:30])[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 3939Lithium HydroxideHCID 8028TetrahydrofuranHCID 67044096[3-(4-Benzenesulfonylthiazol-5-ylmethyl)-5-fluoro-2-methylindol-1-yl]acetic acid methyl ester

生成物 1

HCID 42645097[3-(4-Benzenesulfonylthiazol-5-ylmethyl)-5-fluoro-2-methylindol-1-yl]acetic acid収率 98%

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

実験手順

A mixture of lithium hydroxide (0.10 g), tetrahydrofuran (1.0 mL) and water (1.0 mL) was treated [3-(4-benzenesulfonylthiazol-5-ylmethyl)-5-fluoro-2-methylindol-1-yl]acetic acid methyl ester (0.20 g), and the resulting mixture was stirred at room temperature for 30 minutes. The mixture was diluted with water, concentrated to low bulk under reduced pressure and acidified by the addition of 1.0 M aqueous hydrochloric acid solution. The resulting precipitate was collected by filtration, washed with water and dried to afford the title compound as a white solid (0.19 g).

後処理

  1. concentrationconcentrated to low bulk under reduced pressure
  2. additionacidified by the addition of 1.0 M aqueous hydrochloric acid solution
  3. filtrationThe resulting precipitate was collected by filtration
  4. washwashed with water
  5. customdried

出典と根拠

ORDレコード
ord-f8fad8f3feca4572bfc7a4ca7b0a1e2c
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08394836B2

反応ノート

読み込み中…

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