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Diisopropylethylamine → HCID 57971724、化合物

HRID 2360642
ノート
印刷プレビュー

反応式

HRID 2360642 の反応式
[CH2:1]([O:5][CH:6]([O:8][NH:9][C:10]([CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][C:18]([OH:20])=O)=[O:11])[CH3:7])[CH:2]([CH3:4])[CH3:3].C[Si](C)(C)[O:23][CH2:24][C:25]1[CH:30]=[CH:29][C:28]([NH2:31])=[CH:27][CH:26]=1.C1CN([P+](Br)(N2CCCC2)N2CCCC2)CC1.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C>CN(C=O)C.O.C(OCC)(=O)C>[CH2:1]([O:5][CH:6]([O:8][NH:9][C:10](=[O:11])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][C:18]([NH:31][C:28]1[CH:29]=[CH:30][C:25]([CH2:24][OH:23])=[CH:26][CH:27]=1)=[O:20])[CH3:7])[CH:2]([CH3:3])[CH3:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 81531DiisopropylethylamineHCID 2733179PyBroPHCID 11401321403613-26-3HCID 57971679HCID 57971679、化合物

生成物 1

HCID 57971724HCID 57971724、化合物収率 529.1%

試薬・触媒・溶媒 3

HCID 962Water溶媒
HCID 6228
Dimethylformamide
溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

7-(1-Isobutoxy-ethoxycarbamoyl)-heptanoic acid (5.0 g, 1.72 mmol, 1.0 eq) and 4-trimethylsilanyloxymethyl-phenylamine (3.38 g, 1.72 mmol, 1.0 eq) were stirred together in DMF (140 mL). To the mixture was added PyBroP (10.5 g, 2.25 mmol, 1.3 eq) and DiPEA (3.9 mL, 2.25 mmol, 1.3 eq). The reaction was stirred under a nitrogen atmosphere overnight at room temperature. Ethyl acetate (200 mL) and water (200 mL) were added. The aqueous phase was isolated and re-extracted with ethyl acetate (2×100 mL). The combined organic phases were washed with water (2×50 mL) and brine (50 mL), then dried (MgSO4), filtered and concentrated in vacuo. The crude product was dissolved in the minimum of ethyl acetate and purified by passing through a pad of silica. The product was washed through the silica using ethyl acetate and collected in 100 mL conical flasks until elution ceased by LCMS analysis. Purification gave a yellow oil (3.59 g, 53% yield). LCMS purity 61%, m/z 417 [M++Na]+

後処理

  1. customThe aqueous phase was isolated
  2. extractionre-extracted with ethyl acetate (2×100 mL)
  3. washThe combined organic phases were washed with water (2×50 mL) and brine (50 mL)
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. dissolutionThe crude product was dissolved in the minimum of ethyl acetate
  8. custompurified
  9. washThe product was washed through the silica
  10. customcollected in 100 mL conical flasks until elution
  11. customPurification

出典と根拠

ORDレコード
ord-1800a09a54284b75900489e74ee272c5
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08686032B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート