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5-(hydroxy methyl)-2-propyl-4-(2,5-dimethyl-1H-pyrrol-1-yl)imidazole → 4-(2,5-dimethyl-1H-pyrrol 1-yl)-2-propylimidazole-5-carboxaldehyde

HRID 1197600
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HRID 1197600 반응식
[OH:1][CH2:2][C:3]1[NH:7][C:6]([CH2:8][CH2:9][CH3:10])=[N:5][C:4]=1[N:11]1[C:15]([CH3:16])=[CH:14][CH:13]=[C:12]1[CH3:17]>C1COCC1.O=[Mn]=O>[CH3:17][C:12]1[N:11]([C:4]2[N:5]=[C:6]([CH2:8][CH2:9][CH3:10])[NH:7][C:3]=2[CH:2]=[O:1])[C:15]([CH3:16])=[CH:14][CH:13]=1
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참가 물질

4

반응물 1

HCID 149628935-(hydroxy methyl)-2-propyl-4-(2,5-dimethyl-1H-pyrrol-1-yl)imidazole

생성물 1

HCID 149628924-(2,5-dimethyl-1H-pyrrol 1-yl)-2-propylimidazole-5-carboxaldehyde수율 75%

시약·촉매·용매 2

HCID 14801Manganese dioxide촉매HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 5-(hydroxy-methyl)-2-propyl-4-(2,5-dimethyl-1H-pyrrol-1-yl)imidazole (Example 48, 6.0 g, 0.026 mol) in dry THF (125 mL) was added MnO2 (11.2 g, 0.13 mol) and the reaction mixture refluxed for 4 hours under an atmosphere of nitrogen. The reaction mixture was cooled, filtered through celite, and the resulting filtrate evaporated under reduced pressure. Purification by flash chromatography (silica; 2:1 hexane ethyl acetate) gave the title compound 4-(2,5-dimethyl-1H-pyrrol-1-yl)-2-propylimidazole-5-carboxaldehyde (4.5 g, 75%), mp 119°-121° C.

후처리

  1. temperaturethe reaction mixture refluxed for 4 hours under an atmosphere of nitrogen
  2. temperatureThe reaction mixture was cooled
  3. filtrationfiltered through celite
  4. customthe resulting filtrate evaporated under reduced pressure
  5. customPurification by flash chromatography (silica; 2:1 hexane ethyl acetate)

출처 및 근거

ORD 기록
ord-1424c3f907de4d23add9940af6876df0
출처 데이터셋
uspto-grants-1994_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05276048

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