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HCID 178468689, 화합물 → 4-(3-amino-3-oxopropoxy)-3-[(E)-2-(4-fluorophenyl)ethenyl]-1H-indazole-5-carboxylic acid

HRID 34102
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인쇄 미리보기

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HRID 34102 반응식
C([O:3][C:4]([C:6]1[C:7]([O:24][CH2:25][CH2:26][C:27](=[O:29])[NH2:28])=[C:8]2[C:12](=[CH:13][CH:14]=1)[NH:11][N:10]=[C:9]2/[CH:15]=[CH:16]/[C:17]1[CH:22]=[CH:21][C:20]([F:23])=[CH:19][CH:18]=1)=[O:5])C>S(=O)(=O)(O)O>[C:27]([CH2:26][CH2:25][O:24][C:7]1[C:6]([C:4]([OH:5])=[O:3])=[CH:14][CH:13]=[C:12]2[C:8]=1[C:9](/[CH:15]=[CH:16]/[C:17]1[CH:22]=[CH:21][C:20]([F:23])=[CH:19][CH:18]=1)=[N:10][NH:11]2)(=[O:29])[NH2:28]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 178468689HCID 178468689, 화합물

생성물 1

HCID 600350134-(3-amino-3-oxopropoxy)-3-[(E)-2-(4-fluorophenyl)ethenyl]-1H-indazole-5-carboxylic acid수율 55.1%

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

반응 조건

온도
35 °C

실험 절차

85.3 mg of 4-(2-carbamoylethoxy)-3-[(E)-2-(4-fluorophenyl)-vinyl]-1H-indazole-5-carboxylic acid ethyl ester obtained by Example 763 was dissolved in 3 mL of concentrated sulfuric acid, stirred at 35° C. for 16 hours, and then added with ice under ice cooling. The precipitated crystals were collected by filtration, washed with water, and then dried under reduced pressure, to afford 43.7 mg of the title compound as yellow crude crystals.

후처리

  1. additionadded with ice under ice cooling
  2. filtrationThe precipitated crystals were collected by filtration
  3. washwashed with water
  4. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-c07f796ab20845708b68186787d34af2
출처 데이터셋
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07429609B2

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