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Diisobutylaluminum hydride → 2-methyl-2-(3-phenyl-1H-1,2,4-triazol-5-yl)propan-1-amine

HRID 1397324
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HRID 1397324 반응식
CC(C[AlH]CC(C)C)C.[CH3:10][C:11]([C:15]1[NH:19][N:18]=[C:17]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[N:16]=1)([CH3:14])[C:12]#[N:13]>C1COCC1>[CH3:14][C:11]([C:15]1[NH:19][N:18]=[C:17]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[N:16]=1)([CH3:10])[CH2:12][NH2:13]
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참가 물질

4

반응물 2

HCID 14487Diisobutylaluminum hydrideHCID 67324319HCID 67324319, 화합물

생성물 1

HCID 673242222-methyl-2-(3-phenyl-1H-1,2,4-triazol-5-yl)propan-1-amine수율 87.5%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

DIBAL-H (0.75 mL, 0.75 mmol, 1M in THF) was added to a solution of 2-methyl-2-(3-phenyl-1H-1,2,4-triazol-5-yl)propanenitrile (80 mg, 0.37 mmol) in dry THF (5 mL) at 0° C. The reaction mixture was allowed to warm up to room temperature and further stirred for 2 h. The reaction mixture was then quenched carefully with water and diluted with EtOAc. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford 2-methyl-2-(3-phenyl-1H-1,2,4-triazol-5-yl)propan-1-amine (70 mg, crude), which was carried through without further purification. MS (ESI) m/z: Calculated for C12H16N4: 216.14. found: 217.2 (M+H)+.

후처리

  1. customThe reaction mixture was then quenched carefully with water
  2. additiondiluted with EtOAc
  3. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  4. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-2eadf20b570648d984c1cf59c6d2d049
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08901156B2

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