1,3,3-Trimethyl-2-methyleneindoline → HCID 49845114, 화합물

HRID 537635

반응식

HRID 537635 반응식
[CH2:1]([N:3]([CH2:23][CH2:24][OH:25])[C:4]1[CH:9]=[CH:8][C:7]([C:10]2[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[C:13](=[O:20])[C:12](=[N:21]O)[CH:11]=2)=[CH:6][CH:5]=1)[CH3:2].[CH3:26][N:27]1[C:35]2[C:30](=[CH:31][CH:32]=[CH:33][CH:34]=2)[C:29]([CH3:37])([CH3:36])[C:28]1=[CH2:38]>C(O)C>[CH2:1]([N:3]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[C:13]3[O:20][C:28]4([C:29]([CH3:37])([CH3:36])[C:30]5[C:35](=[CH:34][CH:33]=[CH:32][CH:31]=5)[N:27]4[CH3:26])[CH:38]=[N:21][C:12]=3[CH:11]=2)=[CH:6][CH:5]=1)[CH2:23][CH2:24][OH:25])[CH3:2]

참가 물질

4

반응 조건

온도
100 °C

실험 절차

A suspension of 4-(4-(ethyl(2-hydroxyethyl)amino)phenyl)-2-(hydroxyimino)naphthalen-1(2H)-one (4.0 g, 11.89 mmol) in ethanol (100 ml) was treated with 1,3,3-trimethyl-2-methyleneindoline (2.68 g, 15.46 mmol) in one portion and heated to 100° C. in a sealed tube for 4 hrs. The mixture was then cooled to RT and left to stand overnight. The resulting suspension was evaporated in vacuo to approx 25 ml total volume, MeOH added (25 ml) and the mixture stored in the freezer for 3 hrs. After this time the product was collected by filtration and washed with a little methanol to give the product, 2-(ethyl(4-(1,3,3-trimethylspiro[indoline-2,2′-naphtho[1,2-b][1,4]oxazine]-6′yl)phenyl)amino)ethanol, as pale green fibres (4.15 g, 71%). Analysis of the product by 1H NMR gave a spectrum consistent with the structure.

후처리

  1. temperatureThe mixture was then cooled to RT
  2. waitleft
  3. customThe resulting suspension was evaporated in vacuo to approx 25 ml total volume, MeOH
  4. additionadded (25 ml)
  5. waitthe mixture stored in the freezer for 3 hrs
  6. filtrationAfter this time the product was collected by filtration
  7. washwashed with a little methanol

출처 및 근거

ORD 기록
ord-47a56ca07ce943e7ae9ac17951b04aec
출처 데이터셋
uspto-grants-2014_10
특허 번호
US08865029B2

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