4-Aminopyridine → 1-{4-[4-(3,6-dihydro-2H-pyran-4-yl)-6-morpholin-4-yl-[1,3,5]triazin-2-yl]-phenyl}-3-pyridin-4-yl-urea
反応式
ClC(Cl)(O[C:5](=[O:11])OC(Cl)(Cl)Cl)Cl.[O:13]1[CH2:18][CH:17]=[C:16]([C:19]2[N:24]=[C:23]([N:25]3[CH2:30][CH2:29][O:28][CH2:27][CH2:26]3)[N:22]=[C:21]([C:31]3[CH:36]=[CH:35][C:34]([NH2:37])=[CH:33][CH:32]=3)[N:20]=2)[CH2:15][CH2:14]1.[NH2:38][C:39]1[CH:44]=[CH:43][N:42]=[CH:41][CH:40]=1.CCN(CC)CC>C(Cl)Cl>[O:13]1[CH2:14][CH:15]=[C:16]([C:19]2[N:24]=[C:23]([N:25]3[CH2:26][CH2:27][O:28][CH2:29][CH2:30]3)[N:22]=[C:21]([C:31]3[CH:36]=[CH:35][C:34]([NH:37][C:5]([NH:38][C:39]4[CH:44]=[CH:43][N:42]=[CH:41][CH:40]=4)=[O:11])=[CH:33][CH:32]=3)[N:20]=2)[CH2:17][CH2:18]1参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
To a stirred solution of triphosgene (140 mg, 0.47 mmol) in CH2Cl2 (6 mL) was added 4-[4-(3,6-dihydro-2H-pyran-4-yl)-6-morpholin-4-yl-[1,3,5]triazin-2-yl]-phenylamine (200 mg, 0.59 mmol) at 25° C. The reaction mixture was stirred for 15 min and 4-aminopyridine (166 mg, 1.77 mmol) and NEt3 (814 μL, 5.89 mmol) were added and the reaction mixture was stirred for additional 1 hr. The solvents were distilled and the crude mixture was purified by semi-prep-HPLC (TFA-method) to give 1-{4-[4-(3,6-dihydro-2H-pyran-4-yl)-6-morpholin-4-yl-[1,3,5]triazin-2-yl]-phenyl}-3-pyridin-4-yl-urea (75 mg, 22% yield); MS (ESI) m/z 460
後処理
- stirringthe reaction mixture was stirred for additional 1 hr
- distillationThe solvents were distilled
- customthe crude mixture was purified by semi-prep-HPLC (TFA-method)
出典と根拠
- ORDレコード
- ord-9078012d60814c99926bed2370ddea50
- 出典データセット
- uspto-grants-2012_07
- 特許番号
- US08217036B2
反応ノート
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