Acetonitrile → HCID 62705059、化合物

HRID 1474456ノート

反応式

HRID 1474456 の反応式
[CH2:1]([N:3]([CH2:30][CH3:31])[CH2:4][CH2:5][NH:6][C:7]([C:9]1[C:17]2[CH2:16][CH2:15][CH2:14]/[C:13](=[C:18]3/[C:19](=[O:28])[NH:20][C:21]4[C:26]/3=[CH:25][C:24]([F:27])=[CH:23][CH:22]=4)/[C:12]=2[NH:11][C:10]=1[CH3:29])=[O:8])[CH3:2].C(#N)C.[C:35]([OH:43])(=[O:42])[C@H:36]([CH2:38][C:39]([OH:41])=[O:40])[OH:37]>ClCCl>[C:35]([OH:43])(=[O:42])[C@H:36]([CH2:38][C:39]([OH:41])=[O:40])[OH:37].[CH2:30]([N:3]([CH2:1][CH3:2])[CH2:4][CH2:5][NH:6][C:7]([C:9]1[C:17]2[CH2:16][CH2:15][CH2:14]/[C:13](=[C:18]3/[C:19](=[O:28])[NH:20][C:21]4[C:26]/3=[CH:25][C:24]([F:27])=[CH:23][CH:22]=4)/[C:12]=2[NH:11][C:10]=1[CH3:29])=[O:8])[CH3:31]

参加物

5

反応物 3

HCID 6342AcetonitrileHCID 222656L-Malic AcidHCID 569355771H-Indole-3-carboxamide, N-[2-(diethylamino)ethyl]-7-(5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)-4,5,6,7-tetrahydro-2-methyl-, (7Z)-

生成物 1

HCID 62705059HCID 62705059、化合物収率 93%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

8.49 g (20 mmol) (Z)—N-[2-(diethylamino)ethyl]-2-methyl-7-(1,2-dihydro-5-fluoro-2-oxo-3H-indol-3-ylidene)-4,5,6,7-tetrahydro-1H-indol-3-carboxamide was added to a mixture of 500 ml acetonitrile and 90 ml dichloromethane. The mixture was treated under ultrasonic sound to uniform dispersion. 3.22 g (24 mmol) L-malic acid was added and the solution was heated to reflux with stirring under nitrogen atmosphere. After reaction for 1 h, the resulting solution was filtered while being hot, and the filtrate was concentrated at reduced pressure to dryness, and the resulting product was added to 60 ml anhydrous ethanol and treated under ultrasonic sound to uniform dispersion. Then the solution was filtered, and the filter cake was dried at 40° C. under vacuum, to give the title compound as yellow solid (10.39 g, 18.6 mmol, yield 93%).

後処理

  1. additionThe mixture was treated under ultrasonic sound to uniform dispersion
  2. temperaturethe solution was heated
  3. temperatureto reflux
  4. customAfter reaction for 1 h
  5. filtrationthe resulting solution was filtered
  6. concentrationthe filtrate was concentrated at reduced pressure to dryness
  7. additionthe resulting product was added to 60 ml anhydrous ethanol
  8. additiontreated under ultrasonic sound to uniform dispersion
  9. filtrationThen the solution was filtered
  10. customthe filter cake was dried at 40° C. under vacuum

出典と根拠

ORDレコード
ord-32a0763cbe514b86b2155c1b967f7514
出典データセット
uspto-grants-2015_04
特許番号
US09018242B2

反応ノート

読み込み中…