Water → HCID 178507546、化合物
反応式
[N+:1]([C:4]1[CH:29]=[CH:28][C:7]([CH:8]=[CH:9][C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([CH:16]=[CH:17][C:18]3[CH:23]=[CH:22][C:21]([N+:24]([O-])=O)=[CH:20][CH:19]=3)[N+:11]=2[O-:27])=[CH:6][CH:5]=1)([O-])=O.[S-2].[Na+].[Na+].O>C(O)C>[NH2:24][C:21]1[CH:20]=[CH:19][C:18]([CH:17]=[CH:16][C:12]2[CH:13]=[CH:14][CH:15]=[C:10]([CH:9]=[CH:8][C:7]3[CH:28]=[CH:29][C:4]([NH2:1])=[CH:5][CH:6]=3)[N+:11]=2[O-:27])=[CH:23][CH:22]=1参加物
実験手順
More specifically, the synthesizing procedure is as follows. 2,6-dimethylpyridine or a substituted product thereof, is reacted with p-nitrobenzenealdehyde or a substituted product according to a method described, for example, in Journal of Organic Chemistry, vol. 15, P. 1184 (1950) to synthesize 2,6-di(p-nitrostyryl)pyridine (K). 30 g of this nitro compound is reacted wtih 27 g of m-chloroperbenzoic acid in three liter of dichloromethane to obtain 24 g of 2,6-di(p-nitrostyryl)pyridine-N-oxide. 24 g of this pyridine-N-oxide is reacted with 90 g of sodium sulfide in a solution mixed four liter of water with four liter of ethanol to reduce nitro group selectively and form 18 g of 2,6-di(p-aminostyryl)pyridine-N-oxide (M). The N-oxide amino compound is converted into a diazo compound according to a conventional method, and thereby tetrazonium salt is isolated as 15 g of hydroborofluoric salt (N). 5.0 g of the tetrazonium salt (N) and 5.0 g of 2-hydroxy-3-phenylcarbamoylnaphthalene (O) were dissolved in one liter of DMF, to which aqueous sodium acetate solution (7 g/100 ml) was added to perform coupling reaction. After two hours of stirring, the resultant crystals were separated by filtration, and the crystals were rinsed three times respectively with five liter water, three times respectively with five liter THF, then dried, to obtain 4.0 g of the final product, azo compound (P - 1).
出典と根拠
- ORDレコード
- ord-9de733d0aa844746a233cb060930c6dc
- 出典データセット
- uspto-grants-1989_10
- 特許番号
- US04871633
反応ノート
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