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Isopropanol → trans-2-(2-methyl-2H-indazol-4-yl)cyclopropanecarbaldehyde

HRID 1639753
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HRID 1639753 반응식
[CH3:1][N:2]1[CH:10]=[C:9]2[C:4]([CH:5]=[CH:6][CH:7]=[C:8]2[C@@H:11]2[CH2:13][C@H:12]2[CH2:14][OH:15])=[N:3]1.C[N+]1([O-])CCOCC1.CC(O)C>C(#N)C>[CH3:1][N:2]1[CH:10]=[C:9]2[C:4]([CH:5]=[CH:6][CH:7]=[C:8]2[C@@H:11]2[CH2:13][C@H:12]2[CH:14]=[O:15])=[N:3]1
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참가 물질

5

반응물 3

HCID 3776IsopropanolHCID 82029Methyl morpholine oxideHCID 66720579Trans-[2-(2-methyl-2H-indazol-4-yl)cyclopropyl]methanol

생성물 1

HCID 86641920trans-2-(2-methyl-2H-indazol-4-yl)cyclopropanecarbaldehyde수율 77.2%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

Trans-[2-(2-methyl-2H-indazol-4-yl)cyclopropyl]methanol (500 mg, 2.47 mmol), 4 Å molecular sieves (200 mg), 4-methylmorpholine N-oxide (724 mg, 6.18 mmol) and tetra-n-propylammonium perruthenate(VII) (43.6 mg, 0.124 mmol) were dissolved in acetonitrile (25 mL), and the mixture was stirred at room temperature for 2 hr. 2-Propanol was added, and the mixture was stirred for 30 min. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate) to give the title compound (382 mg, yield 77%).

후처리

  1. stirringthe mixture was stirred for 30 min
  2. customThe solvent was evaporated under reduced pressure
  3. customthe residue was purified by silica gel column chromatography (ethyl acetate)

출처 및 근거

ORD 기록
ord-3b837a79616a4d679ac4944abbfdfdda
출처 데이터셋
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08110585B2

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