1,2-Dichloroethane → 2-(cyclobutylcarbonyl)-N-(tetrahydro-2H-pyran-2-yloxy)-1,2,3,4-tetrahydroisoquinoline-6-carboxamide
反応式
[O:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[O:7][NH:8][C:9]([C:11]1[CH:12]=[C:13]2[C:18](=[CH:19][CH:20]=1)[CH2:17][NH:16][CH2:15][CH2:14]2)=[O:10].[CH:21]1([C:25](O)=[O:26])[CH2:24][CH2:23][CH2:22]1.C1C=CC2N(O)N=NC=2C=1.C(Cl)CCl>CN(C=O)C.C(N(CC)CC)C>[CH:21]1([C:25]([N:16]2[CH2:15][CH2:14][C:13]3[C:18](=[CH:19][CH:20]=[C:11]([C:9]([NH:8][O:7][CH:2]4[CH2:3][CH2:4][CH2:5][CH2:6][O:1]4)=[O:10])[CH:12]=3)[CH2:17]2)=[O:26])[CH2:24][CH2:23][CH2:22]1参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
200 mg of N-(tetrahydro-2H-pyran-2-yloxy)-1,2,3,4-tetrahydroisoquinoline-6-carboxamide, 80 mg of cyclobutan carboxylic acid, 111 mg HOBT, 276 mg EDC and 0.6 ml triethylamine are dissolved in 7 ml DMF and stirred overnight. The mixture is evaporated and the residue is purified by silica gel chromatography. 170 mg of a yellowish foam are obtained.
後処理
- customThe mixture is evaporated
- customthe residue is purified by silica gel chromatography
出典と根拠
- ORDレコード
- ord-24717c4d5bf249158093e90d071f954b
- 出典データセット
- uspto-grants-2013_11
- 特許番号
- US08575193B2
反応ノート
読み込み中…