4-Toluenesulfonyl chloride → 9-Fluoro-6-(p-toluenesulfonyloxy)benzo[g]isoquinoline-5,10-dione

HRID 234811

反応式

HRID 234811 の反応式
C(N(CC)CC)C.[F:8][C:9]1[C:22]2[C:21](=[O:23])[C:20]3[CH:19]=[N:18][CH:17]=[CH:16][C:15]=3[C:14](=[O:24])[C:13]=2[C:12]([OH:25])=[CH:11][CH:10]=1.[Cl:26][C:27]1[C:40]2[C:39](=[O:41])[C:38]3[CH:37]=[N:36][CH:35]=[CH:34][C:33]=3[C:32](=[O:42])[C:31]=2[C:30]([OH:43])=[CH:29][CH:28]=1.[C:44]1([CH3:54])[CH:49]=[CH:48][C:47]([S:50](Cl)(=[O:52])=[O:51])=[CH:46][CH:45]=1>C(Cl)Cl.O>[F:8][C:9]1[C:22]2[C:21](=[O:23])[C:20]3[CH:19]=[N:18][CH:17]=[CH:16][C:15]=3[C:14](=[O:24])[C:13]=2[C:12]([O:25][S:50]([C:47]2[CH:48]=[CH:49][C:44]([CH3:54])=[CH:45][CH:46]=2)(=[O:52])=[O:51])=[CH:11][CH:10]=1.[Cl:26][C:27]1[C:40]2[C:39](=[O:41])[C:38]3[CH:37]=[N:36][CH:35]=[CH:34][C:33]=3[C:32](=[O:42])[C:31]=2[C:30]([O:43][S:50]([C:47]2[CH:48]=[CH:49][C:44]([CH3:54])=[CH:45][CH:46]=2)(=[O:52])=[O:51])=[CH:29][CH:28]=1

参加物

8

反応物 4

HCID 73974-Toluenesulfonyl chlorideHCID 8471TriethylamineHCID 105143529-Fluoro-6-hydroxybenzo[g]isoquinoline-5,10-dioneHCID 107777069-Chloro-6-hydroxybenzo[g]isoquinoline-5,10-dione

生成物 2

HCID 105728809-Fluoro-6-(p-toluenesulfonyloxy)benzo[g]isoquinoline-5,10-dioneHCID 199747549-Chloro-6-(p-toluenesulfonyloxy)benzo[g]isoquinoline-5,10-dione

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6344Dichloromethane溶媒

実験手順

Triethylamine (8.20 mL) is added to a stirred suspension of the 9/1 mixture of 9-fluoro-6-hydroxybenzo[g]isoquinoline-5,10-dione and 9-chloro-6-hydroxybenzo [g]isoquinoline-5,10-dione respectively of Preparative Example 14b (5.53 g) and p-toluenesulfonylchloride (8.47 mL) in methylene chloride (166 mL). The reddish-violet solution obtained is left at room temperature under a nitrogen atmosphere for 1 hour and then it is poured into water (500 mL). The organic phase is separated and the aqueous solution is further extracted with methylene chloride (100 mL). The combined organic solutions are dried (Na2SO4) and concentrated to dryness. The obtained solid is suspended in n-hexane (100 mL) for 1 hour and filtered to give a 9:1 mixture (1H-NMR evaluation) of 9-fluoro-6-(p-toluenesulfonyloxy)benzo [g]isoquinoline-5,10-dione and 9-chloro-6-(p-toluenesulfonyloxy)benzo[g]iso quinoline-5,10-dione respectively (8.85 g).

後処理

  1. customThe reddish-violet solution obtained
  2. customThe organic phase is separated
  3. extractionthe aqueous solution is further extracted with methylene chloride (100 mL)
  4. dry with materialThe combined organic solutions are dried (Na2SO4)
  5. concentrationconcentrated to dryness
  6. waitThe obtained solid is suspended in n-hexane (100 mL) for 1 hour
  7. filtrationfiltered

出典と根拠

ORDレコード
ord-e2c2bbc75c0841fbbc9018ec4040fd67
出典データセット
uspto-grants-1997_01
特許番号
US05596097

関連ノート

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