反応式
[N:1]1[CH:6]=[CH:5][C:4]([CH:7]2[C:15](=[O:16])[C:14]3[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=3)[C:8]2=O)=[N:3][CH:2]=1.O.[NH2:19][NH2:20]>C(O)C>[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][C:8]2[C:9]3[C:14](=[CH:13][CH:12]=[CH:11][CH:10]=3)[C:15](=[O:16])[NH:20][N:19]=2)=[N:3][CH:2]=1参加物
4
実験手順
1.20 g (5.35 mmol) 2-pyrimidin-4-yl-indan-1,3-dione in 30 ml ethanol is spiked with 345 μl (6.96 mmol) hydrazine hydrate and heated for 5 h to 100° C. After cooling, the product is filtered off and washed with ethanol: m.p.: 204-206° C.; Anal. calc.(C13H10N4O.0.5 H2O) C, 63.15%; H, 4.48%; N, 22.66%; found C, 63.3%; H, 4.5%; N, 22.7%; FAB MS (M+H)+=239.
後処理
- temperatureheated for 5 h to 100° C
- temperatureAfter cooling
- filtrationthe product is filtered off
- washwashed with ethanol
出典と根拠
- ORDレコード
- ord-1f02f0f7de3640f19bbc8cc64a2f898f
- 出典データセット
- uspto-grants-2003_02
- 特許番号
- US06514974B2
関連ノート
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