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Potassium Hydroxide → 3-(4-Fluorophenyl)imidazo[1,5-a]pyridine-8-carboxylic acid

HRID 1423014
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반응식

HRID 1423014 반응식
C([O:3][C:4]([C:6]1[C:7]2[N:8]([C:12]([C:15]3[CH:20]=[CH:19][C:18]([F:21])=[CH:17][CH:16]=3)=[N:13][CH:14]=2)[CH:9]=[CH:10][CH:11]=1)=[O:5])C.[OH-].[K+]>CO.O>[F:21][C:18]1[CH:17]=[CH:16][C:15]([C:12]2[N:8]3[CH:9]=[CH:10][CH:11]=[C:6]([C:4]([OH:5])=[O:3])[C:7]3=[CH:14][N:13]=2)=[CH:20][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14797Potassium HydroxideHCID 683454063-(4-Fluorophenyl)-imidazo[1,5-a]pyridine-8-carboxylic acid ethyl ester

생성물 1

HCID 671947383-(4-Fluorophenyl)imidazo[1,5-a]pyridine-8-carboxylic acid

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

To a solution of 3-(4-fluorophenyl)-imidazo[1,5-a]pyridine-8-carboxylic acid ethyl ester (290 mg, 1.0 mmol) in methanol (20 mL) is added a solution of 85% potassium hydroxide pellets (0.300 g, 3.92 mmol) in water (5.0 mL). The reaction mixture is warmed at reflux for 5 minutes, cooled to room temperature and concentrated in vacuo to remove excess methanol. The mixture is acidified to pH 4 with 1 N aqueous HCl and the resulting precipitate is collected by filtration, washed with water and dried to afford the title product.

후처리

  1. temperatureThe reaction mixture is warmed
  2. temperatureat reflux for 5 minutes
  3. concentrationconcentrated in vacuo
  4. customto remove excess methanol
  5. filtrationthe resulting precipitate is collected by filtration
  6. washwashed with water
  7. customdried

출처 및 근거

ORD 기록
ord-380ca5d6c7674347bcf1da703b2421a6
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08927550B2

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