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5-(N-t-butoxycarbonylindol-2-yl)-2-methyl-1-(tetrahydropyran-4-yl)benzimidazole → HCID 67497943、化合物

HRID 74206
ノート
印刷プレビュー

反応式

HRID 74206 の反応式
C(OC([N:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]=[C:9]1[C:17]1[CH:32]=[CH:31][C:20]2[N:21]([CH:25]3[CH2:30][CH2:29][O:28][CH2:27][CH2:26]3)[C:22]([CH3:24])=[N:23][C:19]=2[CH:18]=1)=O)(C)(C)C>Cl>[NH:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]=[C:9]1[C:17]1[CH:32]=[CH:31][C:20]2[N:21]([CH:25]3[CH2:26][CH2:27][O:28][CH2:29][CH2:30]3)[C:22]([CH3:24])=[N:23][C:19]=2[CH:18]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 674982575-(N-t-butoxycarbonylindol-2-yl)-2-methyl-1-(tetrahydropyran-4-yl)benzimidazole

生成物 1

HCID 67497943HCID 67497943、化合物

試薬・触媒・溶媒 1

HCID 313Hydrochloric Acid溶媒

実験手順

5-(N-t-butoxycarbonylindol-2-yl)-2-methyl-1-(tetrahydropyran-4-yl)benzimidazole (see Synthesis Example 37 (200 mg, 0.463 mmol) was added to a 1N aqueous hydrochloric acid solution (10 mL), and this was stirred at room temperature for 3 hours. After the reaction was complete, this was allowed to stand for 3 days and the precipitated crystals were filtered off, and to this was added saturated aqueous sodium hydrogen carbonate (5 mL) and this was stirred for 30 minutes. The precipitated crystals were filtered off, washed with water and dried to yield the title compound (155 mg, quant.) as light brown crystals.

後処理

  • waitto stand for 3 days
  • filtrationthe precipitated crystals were filtered off
  • additionto this was added saturated aqueous sodium hydrogen carbonate (5 mL)
  • stirringthis was stirred for 30 minutes
  • filtrationThe precipitated crystals were filtered off
  • washwashed with water
  • customdried
  • 出典と根拠

    ORDレコード
    ord-1cd7e1f954d44114a1fde5ccb2fe9a68
    出典データセット
    uspto-grants-2014_09
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US08829035B2

    反応ノート

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