反応式
[CH:1]1[CH:6]=[C:5]([NH:7][C:8]2[N:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[N:4]=[CH:3][CH:2]=1.[OH-].[K+].I[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH3:34]>CN(C)C=O>[CH2:34]([N:7]([C:5]1[CH:6]=[CH:1][CH:2]=[CH:3][N:4]=1)[C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][N:13]=1)[CH2:33][CH2:32][CH2:31][CH2:30][CH2:29][CH2:28][CH2:27][CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][CH3:17]参加物
5
実験手順
To a flask were added 1.0 g 2,2′-dipyridylamine, 1.0 g of pulverized potassium hydroxide and 15 ml of N,N-dimethylformamide. After stirring for 1 hour under nitrogen, the mixture was cooled to 5 C and 2.2 g of 1-iodooctadecane were added. The mixture was allowed to warm to 22 C and stirred for 16 hours, then heated to 40 C for 2 hours. After quenching with 25 ml water and cooling to 22 C, the product was filtered and washed with water. The product was dissolved in 25 ml hot ethanol with 100 mg activated carbon, stirred for 30 minutes and filtered through celite. After adding 25 ml water and cooling to 5 C, the product was filtered, washed with water and dried leaving 2.1 g light yellow solid.
後処理
- additionwere added
- temperatureto warm to 22 C
- stirringstirred for 16 hours
- temperatureheated to 40 C for 2 hours
- customAfter quenching with 25 ml water
- temperaturecooling to 22 C
- filtrationthe product was filtered
- washwashed with water
- dissolutionThe product was dissolved in 25 ml hot ethanol with 100 mg
- stirringstirred for 30 minutes
- filtrationfiltered through celite
- additionAfter adding 25 ml water
- temperaturecooling to 5 C
- filtrationthe product was filtered
- washwashed with water
- customdried
- customleaving 2.1 g light yellow solid
出典と根拠
- ORDレコード
- ord-9a1d73b8a7ca4f36b2885474a8a54016
- 出典データセット
- uspto-grants-2009_05
- 特許番号
- US07538931B2
関連ノート
読み込み中…