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Imidazole → 1-(2-{[tert-butyl(dimethyl)silyl]oxy}-1,1-dimethylethyl)-3-iodo-1H-pyrrolo[3,2-c]pyridine

HRID 1753068
ノート
印刷プレビュー

反応式

HRID 1753068 の反応式
[I:1][C:2]1[C:6]2[CH:7]=[N:8][CH:9]=[CH:10][C:5]=2[N:4]([C:11]([CH3:15])([CH3:14])[CH2:12][OH:13])[CH:3]=1.N1C=CN=C1.[CH3:21][C:22]([Si:25](Cl)([CH3:27])[CH3:26])([CH3:24])[CH3:23]>C(Cl)Cl>[NH3:4].[Si:25]([O:13][CH2:12][C:11]([N:4]1[C:5]2[CH:10]=[CH:9][N:8]=[CH:7][C:6]=2[C:2]([I:1])=[CH:3]1)([CH3:15])[CH3:14])([C:22]([CH3:24])([CH3:23])[CH3:21])([CH3:27])[CH3:26]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 795ImidazoleHCID 28928tert-Butyldimethylsilyl chlorideHCID 900938832-(3-iodo-1H-pyrrolo[3,2-c]pyridin-1-yl)-2-methylpropan-1-ol

生成物 2

HCID 222AmmoniaHCID 900934361-(2-{[tert-butyl(dimethyl)silyl]oxy}-1,1-dimethylethyl)-3-iodo-1H-pyrrolo[3,2-c]pyridine収率 148.5%

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒

実験手順

To a suspension of 2-(3-iodo-1H-pyrrolo[3,2-c]pyridin-1-yl)-2-methylpropan-1-ol (Preparation 66, 3.86 g, 12.2 mmol) in DCM (50 mL) was added imidazole (2.08 g, 30.5 mmol) followed by TBDMSCl (2.21 g, 14.7 mmol) and the reaction was stirred at room temperature for 18 hours. The reaction was partitioned between water (30 mL) and DCM (40 mL). The aqueous layer was washed twice with DCM (40 mL), the organic layers combined, dried and concentrated in vacuo. The residue was purified using silica gel column chromatography eluting with 30% EtOAc in heptanes followed by 80:20:2 EtOAc:MeOH:NH3 to afford the title compound as a colourless oil (3.90 g, 74%).

後処理

  1. customThe reaction was partitioned between water (30 mL) and DCM (40 mL)
  2. washThe aqueous layer was washed twice with DCM (40 mL)
  3. customdried
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified
  6. washeluting with 30% EtOAc in heptanes

出典と根拠

ORDレコード
ord-5da4ee6cc143422295e829ee61334180
出典データセット
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09163021B2

反応ノート

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