Isatoic Anhydride → HCID 13365992、化合物
反応式
[NH2:1][CH2:2][CH2:3][CH2:4][N:5]1[CH2:10][CH2:9][N:8]([C:11]2[N:16]=[CH:15][CH:14]=[CH:13][N:12]=2)[CH2:7][CH2:6]1.[C:17]12[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=1)[NH:22]C(=O)O[C:18]2=[O:19].C(OCC)(=O)C>CN(C)C=O.O>[N:16]1[CH:15]=[CH:14][CH:13]=[N:12][C:11]=1[N:8]1[CH2:7][CH2:6][N:5]([CH2:4][CH2:3][CH2:2][NH:1][C:18](=[O:19])[C:17]2[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=2[NH2:22])[CH2:10][CH2:9]1参加物
6
実験手順
0.02 mol of 1-(3-aminopropyl)-4-(2-pyrimidinyl)piperazine is dissolved in 100 ml of absolute dimethylformamide, 0.02 mol of isatoic anhydride is added, and the mixture is stirred for 1 hour. It is diluted with 50 ml of water, shaken with ethyl acetate and the organic phase is evaporated. Purification is by column chromatography over silica gel 60. After elution with methylene chloride/methanol 93:7, the resulting oil can be crystallised from ethyl acetate with isopropyl ether.
後処理
- customthe organic phase is evaporated
- customPurification
- washAfter elution with methylene chloride/methanol 93:7
- customthe resulting oil can be crystallised from ethyl acetate with isopropyl ether
出典と根拠
- ORDレコード
- ord-98824a1aa9d64cd99dfc627f8dc93b0a
- 出典データセット
- uspto-grants-1993_02
- 特許番号
- US05187276
反応ノート
読み込み中…