Water → HCID 44252387、化合物

HRID 1477184ノート

反応式

HRID 1477184 の反応式
[CH2:1]([C:8]1([CH2:19][N:20]([CH3:22])[CH3:21])[CH2:13][CH2:12][C:11]([N:16]([CH3:18])[CH3:17])([C:14]#N)[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:23]1([Mg]Cl)[CH:28]=[CH:27]C=[CH:25][CH:24]=1.[NH4+].[Cl-].O>C1COCC1>[CH2:1]([C:8]1([CH2:19][N:20]([CH3:21])[CH3:22])[CH2:13][CH2:12][C:11]([N:16]([CH3:17])[CH3:18])([C:14]2[CH:27]=[CH:28][CH:23]=[CH:24][CH:25]=2)[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

6

反応物 4

HCID 962WaterHCID 25517Ammonium ChlorideHCID 686314524-Benzyl-1-(dimethylamino)-4-((dimethylamino)methyl)cyclohexane carbonitrileHCID 178478979HCID 178478979、化合物

生成物 1

HCID 44252387HCID 44252387、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

The title compound of step 1 (0.88 g, 2.94 mmol) was dissolved in THF (35 mL) and mixed in drops with 2M phenylmagnesium chloride solution (5.1 mL, 10.2 mmol) with ice cooling. The reaction solution was heated to boiling for 8 h. For work up the solution was mixed with 20% NH4Cl solution (0.6 mL) and water (0.4 mL) with ice cooling, extracted with ether (3×25 mL), the ether solution was washed with water, dried (Na2SO4) and concentrated to low volume in a vacuum. The residue was purified by column chromatography with EtOH/EE (1:20). 2 fractions were obtained, wherein according to LCMS, inter alia, the more polar fraction (300 mg) contained the desired substance.

後処理

  1. temperatureThe reaction solution was heated
  2. extractionextracted with ether (3×25 mL)
  3. washthe ether solution was washed with water
  4. dry with materialdried (Na2SO4)
  5. concentrationconcentrated to low volume in a vacuum
  6. customThe residue was purified by column chromatography with EtOH/EE (1:20)
  7. custom2 fractions were obtained

出典と根拠

ORDレコード
ord-cd4c1ad24bee4d3e80470eaff39787ce
出典データセット
uspto-grants-2016_08
特許番号
US09403767B2

反応ノート

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