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Hydrochloric Acid → 2-(3-fluoro-phenyl)-6-methoxy-pyrazolo[1,5-b]pyridazine-3-carboxylic Acid

HRID 1280411
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반응식

HRID 1280411 반응식
[OH-].[Na+].C[O:4][C:5]([C:7]1[C:8]([C:18]2[CH:23]=[CH:22][CH:21]=[C:20]([F:24])[CH:19]=2)=[N:9][N:10]2[C:15]=1[CH:14]=[CH:13][C:12]([O:16][CH3:17])=[N:11]2)=[O:6].Cl>C(O)C>[F:24][C:20]1[CH:19]=[C:18]([C:8]2[C:7]([C:5]([OH:6])=[O:4])=[C:15]3[N:10]([N:11]=[C:12]([O:16][CH3:17])[CH:13]=[CH:14]3)[N:9]=2)[CH:23]=[CH:22][CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 570178562-(3-fluoro-phenyl)-6-methoxy-pyrazolo[1,5-b]pyridazine-3-carboxylic Acid Methyl Ester

생성물 1

HCID 225623402-(3-fluoro-phenyl)-6-methoxy-pyrazolo[1,5-b]pyridazine-3-carboxylic Acid수율 91.2%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

2N sodium hydroxide (50 ml) was added to a solution of 2-(3-fluoro-phenyl)-6-methoxy-pyrazolo[1,5-b]pyridazine-3-carboxylic acid methyl ester (2.3 g) in absolute ethanol (50 ml) and the resulting mixture heated to reflux for three hours. The cooled reaction mixture was poured slowly into a stirred solution of 2N hydrochloric acid (300 ml). The resulting suspension was stirred at ambient temperature for 1 hour then filtered and the filter cake washed with water and dried in vacuo at 600 to give the title compound as an off-white solid (2.0 g, 91%).

후처리

  1. temperaturethe resulting mixture heated
  2. temperatureto reflux for three hours
  3. customThe cooled reaction mixture
  4. filtrationthen filtered
  5. washthe filter cake washed with water
  6. customdried in vacuo at 600

출처 및 근거

ORD 기록
ord-0f7df32302da4c72a135d818eb4f73e2
출처 데이터셋
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06451794B1

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