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Sodium Hydroxide → 5-(4-Carboxybuta-1,3-dienyl)-imidazo[1,5-a]pyridine

HRID 280203
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인쇄 미리보기

반응식

HRID 280203 반응식
C([O:3][C:4]([CH:6]=[CH:7][CH:8]=[CH:9][C:10]1[N:15]2[CH:16]=[N:17][CH:18]=[C:14]2[CH:13]=[CH:12][CH:11]=1)=[O:5])C.[OH-].[Na+]>CO>[C:4]([CH:6]=[CH:7][CH:8]=[CH:9][C:10]1[N:15]2[CH:16]=[N:17][CH:18]=[C:14]2[CH:13]=[CH:12][CH:11]=1)([OH:5])=[O:3]
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 539135015-(4-Ethoxycarbonylbuta-1,3-dienyl)imidazo[1,5-a]pyridine

생성물 1

HCID 538381615-(4-Carboxybuta-1,3-dienyl)-imidazo[1,5-a]pyridine

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 200 mg of 5-(4-ethoxycarbonylbuta-1,3-dienyl)imidazo[1,5-a]pyridine in 20 ml of methanol is added 4 ml of 1N sodium hydroxide. The reaction mixture is stirred at room temperature for 18 hours. The methanol is evaporated under reduced pressure and the residue diluted with 20 ml of water and the solution is adjusted to pH 5 with hydrochloric acid. The precipitate is collected to give 5-(4-carboxybuta-1,3-dienyl)-imidazo[1,5-a]pyridine, melting at 243°-245°.

후처리

  1. customThe methanol is evaporated under reduced pressure
  2. additionthe residue diluted with 20 ml of water
  3. customThe precipitate is collected

출처 및 근거

ORD 기록
ord-7e00622a39854c5db365d0fb36351fff
출처 데이터셋
uspto-grants-1986_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04588732

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