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Methanol → 5-(p-Hydroxymethylphenyl)imidazo[1,5-a]pyridine

HRID 477982
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반응식

HRID 477982 반응식
C([O:3][C:4]([C:6]1[CH:11]=[CH:10][C:9]([C:12]2[N:17]3[CH:18]=[N:19][CH:20]=[C:16]3[CH:15]=[CH:14][CH:13]=2)=[CH:8][CH:7]=1)=O)C.[H-].C([Al+]CC(C)C)C(C)C.C1(C)C=CC=CC=1.CO>C(Cl)Cl>[OH:3][CH2:4][C:6]1[CH:7]=[CH:8][C:9]([C:12]2[N:17]3[CH:18]=[N:19][CH:20]=[C:16]3[CH:15]=[CH:14][CH:13]=2)=[CH:10][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 887MethanolHCID 1140TolueneHCID 13649431ethyl 4-(H-imidazo[1,5-a]pyridin-5-yl)benzoateHCID 21225700Diisobutylaluminumhydride

생성물 1

HCID 136494325-(p-Hydroxymethylphenyl)imidazo[1,5-a]pyridine

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

1 g of 5-(p-ethoxycarbonylphenyl)imidazo[1,5-a]pyridine is dissolved in 26 ml of methylene chloride at -78° under nitrogen, and then 6.6 ml of diisobutylaluminium hydride in toluene (11.4 mmole) is added dropwise. After stirring for 1 h, 1.5 ml of methanol is added, the cold bath is removed and 15 ml of water is added. The salts are filtered off, the organic phase is dried over sodium sulfate and evaporated to yield the title compound, m.p. 137°-138°.

후처리

  1. customthe cold bath is removed
  2. addition15 ml of water is added
  3. filtrationThe salts are filtered off
  4. dry with materialthe organic phase is dried over sodium sulfate
  5. customevaporated

출처 및 근거

ORD 기록
ord-7b0bd7b0db7f45769f332c652db1dfb3
출처 데이터셋
uspto-grants-1989_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04889861

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