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

HRID 1944483
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HRID 1944483 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

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

생성물 1

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

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-f8fad8f3feca4572bfc7a4ca7b0a1e2c
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08394836B2

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