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Diisobutylaluminum hydride → (3-iodo-1-methyl-1H-indazol-5-yl)methanol

HRID 246338
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HRID 246338 반응식
C[O:2][C:3]([C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][CH:13]=1)[N:10]([CH3:14])[N:9]=[C:8]2[I:15])=O.CC(C[AlH]CC(C)C)C>C(Cl)Cl>[I:15][C:8]1[C:7]2[C:11](=[CH:12][CH:13]=[C:5]([CH2:3][OH:2])[CH:6]=2)[N:10]([CH3:14])[N:9]=1
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참가 물질

4

반응물 2

HCID 14487Diisobutylaluminum hydrideHCID 71279594Methyl 3-iodo-1-methyl-1H-indazole-5-carboxylate

생성물 1

HCID 71280092(3-iodo-1-methyl-1H-indazol-5-yl)methanol수율 93.4%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
0 °C

실험 절차

To a solution of 3-iodo-1-methyl-1H-indazole-5-carboxylic acid methyl ester (0.95 g, 3.01 mmol) in CH2Cl2 (30 mL) at 0° C. was slowly added DIBAL-H (1.18 mL, 6.61 mmol). The reaction mixture was stirred at 0° C. for 1.5 h. Carefully quenched with MeOH (1 mL) then diluted with CH2Cl2 (20 mL) and added saturated aqueous Na+K+ tartrate (30 mL). The biphasic mixture was stirred vigorously at room temp for 1 h. The layers were separated and the aqueous phase was extracted with CH2Cl2. The combined organics were washed with water then dried over MgSO4 and concentrated to afford 810 mg of (3-iodo-1-methyl-1H-indazol-5-yl)methanol as a yellow waxy solid.

후처리

  1. customat 0° C.
  2. customCarefully quenched with MeOH (1 mL)
  3. additionthen diluted with CH2Cl2 (20 mL)
  4. additionadded saturated aqueous Na+K+ tartrate (30 mL)
  5. stirringThe biphasic mixture was stirred vigorously at room temp for 1 h
  6. customThe layers were separated
  7. extractionthe aqueous phase was extracted with CH2Cl2
  8. washThe combined organics were washed with water
  9. dry with materialthen dried over MgSO4
  10. concentrationconcentrated

출처 및 근거

ORD 기록
ord-2bc6f15d51aa4840af5cc95f4a7e8df8
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08658646B2

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