1-(benzyloxymethyl)-1H-tetrazole → 4-((1-(benzyloxymethyl)-1H-tetrazol-5-yl)(5-ethoxy-2-fluoro-3-isopropoxyphenyl)methylamino)benzonitrile

HRID 2104953노트

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HRID 2104953 반응식
[CH2:1]([O:8][CH2:9][N:10]1[CH:14]=[N:13][N:12]=[N:11]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Li]CCCC.[CH2:20]([O:22][C:23]1[CH:24]=[C:25]([O:40][CH:41]([CH3:43])[CH3:42])[C:26]([F:39])=[C:27]([CH:38]=1)/[CH:28]=[N:29]/[C:30]1[CH:37]=[CH:36][C:33]([C:34]#[N:35])=[CH:32][CH:31]=1)[CH3:21]>C1COCC1>[CH2:1]([O:8][CH2:9][N:10]1[C:14]([N:29]([CH2:28][C:27]2[CH:38]=[C:23]([O:22][CH2:20][CH3:21])[CH:24]=[C:25]([O:40][CH:41]([CH3:43])[CH3:42])[C:26]=2[F:39])[C:30]2[CH:37]=[CH:36][C:33]([C:34]#[N:35])=[CH:32][CH:31]=2)=[N:13][N:12]=[N:11]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

참가 물질

5

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온도
-78 °C

실험 절차

To a solution of Intermediate 12.1 (50.0 mg, 0.263 mmol) in 2 mL THF at −78° C. was added 1.6 M solution of BuLi in THF (181 μL, 0.289 mmol). The mixture was stirred at −78° C. for 2 min, then a solution of Intermediate 7.3 (86 mg, 0.263 mmol) in 0.6 mL THF was added dropwise. The mixture was stirred at −78° C. for 30 min, was allowed to warm to rt over 1 h, then was quenched with sat. NH4Cl. The mixture was diluted with EtOAc, washed with H2O and brine, dried (Na2SO4) and concentrated. The crude product was purified by flash chromatography (25 to 30% EtOAc/hexanes, stepwise gradient) to afford 33 mg of Intermediate 12.2 as yellow residue.

후처리

  1. stirringThe mixture was stirred at −78° C. for 30 min
  2. temperatureto warm to rt over 1 h
  3. customwas quenched with sat. NH4Cl
  4. additionThe mixture was diluted with EtOAc
  5. washwashed with H2O and brine
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated
  8. customThe crude product was purified by flash chromatography (25 to 30% EtOAc/hexanes, stepwise gradient)

출처 및 근거

ORD 기록
ord-3e94b99a5adc492fbcab42fc6c24c872
출처 데이터셋
uspto-grants-2009_08
특허 번호
US07576098B2

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