Imidazole → (S)-3-[(4-Iodomethyl-phenyl)-(tetrahydro-pyran-2-yloxy)-methyl]-benzonitrile

HRID 1717720ノート

反応式

HRID 1717720 の反応式
O[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([C@H:9]([O:18][CH:19]2[CH2:24][CH2:23][CH2:22][CH2:21][O:20]2)[C:10]2[CH:11]=[C:12]([CH:15]=[CH:16][CH:17]=2)[C:13]#[N:14])=[CH:5][CH:4]=1.[I:25]I.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N1C=CN=C1.S([O-])([O-])(=O)=S.[Na+].[Na+]>ClCCl>[I:25][CH2:2][C:3]1[CH:8]=[CH:7][C:6]([C@H:9]([O:18][CH:19]2[CH2:24][CH2:23][CH2:22][CH2:21][O:20]2)[C:10]2[CH:11]=[C:12]([CH:15]=[CH:16][CH:17]=2)[C:13]#[N:14])=[CH:5][CH:4]=1

参加物

7

実験手順

Add sequentially a solution of (S)-3-[(4-hydroxymethyl-phenyl)-(tetrahydro-pyran-2-yloxy)-methyl]-benzonitrile (2.0 g, 6.18 mmol) dichloromethane (20 ml) and a solution of iodine (1.72 g, 6.80 mmol) in dichloromethane (30 ml) to a cooled (0° C.) solution of triphenylphosphine (1.78 g, 6.80 mmol) and imidazole (635 mg, 9.33 mmol) in dichloromethane (20 ml). Allow to warm to room temperature, then stir for 1.5 hours. Pour the mixture into a cold (0° C.) solution of sodium thiosulfate (3.63 g, 23 mmol) in an ice/water mixture (250 g) and stir for 30 minutes. Extract the aqueous layer with dichloromethane (30 ml). Combine the organic extracts and wash with water, dry with sodium sulfate, filter and concentrate. Purify the crude product via silica chromatography eluting with 15:85 ethyl acetate:hexanes to give the title compound (2.19 g, 82%). MS (m/z). Parent ion not observed.

後処理

  1. stirringstir for 30 minutes
  2. extractionExtract the aqueous layer with dichloromethane (30 ml)
  3. washCombine the organic extracts and wash with water
  4. dry with materialdry with sodium sulfate
  5. filtrationfilter
  6. concentrationconcentrate
  7. customPurify the crude product via silica chromatography
  8. washeluting with 15:85 ethyl acetate

出典と根拠

ORDレコード
ord-47e03eaf11cb4cdda51e8c849bdb6172
出典データセット
uspto-grants-2010_09
特許番号
US07803938B2

反応ノート

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