2-Dimethylaminopyridine → HCID 14304997、化合物

HRID 477057ノート

反応式

HRID 477057 の反応式
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[N:7]1[CH2:12][CH2:11][N:10]([CH2:13][CH2:14][CH2:15][CH2:16][NH2:17])[CH2:9][CH2:8]1.[O:18]1[C:28]2[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=2)[C:21](=[O:22])[C:20]([C:29](O)=[O:30])=[C:19]1[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1.CN(C1C=CC=CN=1)C.CS(Cl)(=O)=O>ClCCl>[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[N:7]1[CH2:8][CH2:9][N:10]([CH2:13][CH2:14][CH2:15][CH2:16][NH:17][C:29]([C:20]2[C:21](=[O:22])[C:23]3[C:28](=[CH:27][CH:26]=[CH:25][CH:24]=3)[O:18][C:19]=2[C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)=[O:30])[CH2:11][CH2:12]1

参加物

6

反応物 4

HCID 218852-DimethylaminopyridineHCID 31297Methanesulfonyl chlorideHCID 12674946HCID 12674946、化合物HCID 14295622HCID 14295622、化合物

生成物 1

HCID 14304997HCID 14304997、化合物収率 64.8%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

3.6 g of the 4-[4-(2-pyridyl)-piperazin-1-yl]butylamine obtained above were added to a reaction mixture cooled to -2020 C. which contained, in 100 ml of absolute dichloromethane, a mixed anhydride produced in a manner analogous to Example 1 (a) from 4.0 g flavone-3-carboxylic acid, 3.367 g dimethylaminopyridine and 1.28 ml methanesulfonyl chloride. The reaction mixture was allowed to warm up to room temperature and stirred at room temperature for two hours. Subsequently the reaction mixture was worked up analogously to Example 3, and the resulting title compound was recrystallized from ethylacetate. There were obtained 4.7 g 3-{4-[4-(2-pyridyl)-piperazin-1-yl]-butylaminocarbonyl}flavone.

後処理

  1. additionabove were added to a reaction mixture
  2. temperaturecooled to -2020 C
  3. customthe resulting title compound was recrystallized from ethylacetate

出典と根拠

ORDレコード
ord-9ada4ac23ead42588bc52fa437a22f17
出典データセット
uspto-grants-1989_12
特許番号
US04886806

反応ノート

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