Iodine chloride → 2-iodo-4-[1-methyl-3-(4-nitrophenyl)-1H-pyrazol-4-yl]-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine

HRID 29005노트

반응식

HRID 29005 반응식
[I:1]Cl.[CH3:3][N:4]1[CH:8]=[C:7]([C:9]2[CH:14]=[CH:13][N:12]=[C:11]3[N:15]([S:22]([C:25]4[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=4)(=[O:24])=[O:23])[C:16]([Si](C)(C)C)=[CH:17][C:10]=23)[C:6]([C:31]2[CH:36]=[CH:35][C:34]([N+:37]([O-:39])=[O:38])=[CH:33][CH:32]=2)=[N:5]1>C(#N)C>[I:1][C:16]1[N:15]([S:22]([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)(=[O:24])=[O:23])[C:11]2=[N:12][CH:13]=[CH:14][C:9]([C:7]3[C:6]([C:31]4[CH:36]=[CH:35][C:34]([N+:37]([O-:39])=[O:38])=[CH:33][CH:32]=4)=[N:5][N:4]([CH3:3])[CH:8]=3)=[C:10]2[CH:17]=1

참가 물질

4

반응 조건

온도
-10 °C

실험 절차

To a solution of ICl (1M in CH2Cl2, 43.3 mmol) in acetonitrile (250 ml) at −10° C. was added a solution of 4-[1-methyl-3-(4-nitrophenyl)-1H-pyrazol-4-yl]-1-(phenylsulfonyl)-2-(trimethylsilyl)-1H-pyrrolo[2,3-b]pyridine (8.67 mmol) in acetonitrile (46 ml) followed by stirring at −10° C. for 5 minutes. The reaction was concentrated to approx. ⅓ total volume and then diluted with EtOAc (500 ml). The solution was washed with saturated NaHCO3(aq) (100 ml), saturated Na2S2O3(aq) (100 ml), brine (100 ml), and dried over MgSO4. Filtration and concentration in vacuo yielded a tan solid which was triturated with hot acetonitrile/Et2O, providing the title product as a light tan solid (53%). ESMS [M+H]+: 586.0.

후처리

  1. concentrationThe reaction was concentrated to approx. ⅓ total volume
  2. additiondiluted with EtOAc (500 ml)
  3. washThe solution was washed with saturated NaHCO3(aq) (100 ml), saturated Na2S2O3(aq) (100 ml), brine (100 ml)
  4. dry with materialdried over MgSO4
  5. filtrationFiltration and concentration in vacuo
  6. customyielded a tan solid which
  7. customwas triturated with hot acetonitrile/Et2O

출처 및 근거

ORD 기록
ord-9e42a0feeb354792b99966e56e2c90d9
출처 데이터셋
uspto-grants-2008_09
특허 번호
US07419988B2

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