Pyridine → N-[5-(cyclohexylamino)[1,2,4]triazolo[1,5-a]pyridin-2-yl]-2-pyridin-3-ylacetamide
反応式
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][C:8](Cl)=[O:9])[CH:2]=1.[CH:11]1([NH:17][C:18]2[N:23]3[N:24]=[C:25]([NH2:27])[N:26]=[C:22]3[CH:21]=[CH:20][CH:19]=2)[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]1.N1C=CC=CC=1.CCOCC>C(Cl)Cl.O>[CH:11]1([NH:17][C:18]2[N:23]3[N:24]=[C:25]([NH:27][C:8](=[O:9])[CH2:7][C:3]4[CH:2]=[N:1][CH:6]=[CH:5][CH:4]=4)[N:26]=[C:22]3[CH:21]=[CH:20][CH:19]=2)[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16]1参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
反応条件
- 温度
- 55 °C
実験手順
A mixture of pyridin-3-ylacetyl chloride (120.07 mg; 0.77 mmol; 1.50 eq.) and N5-cyclohexyl[1,2,4]triazolo[1,5-a]pyridine-2,5-diamine ((A9); 119 mg; 0.51 mmol; 1.0 eq.) in DCM (1 mL) in presence of pyridine (1244; 1.54 mmol; 3 eq.) was heated in a sealed tube at 55° C. for 3 h. Et2O and Water were then added to the mixture, the precipitate obtained was filtered, washed with water, Et2O, Acetonitrile and dried under vacuum at 40° C. to give the title compound as an off-white powder (74 mg, 41%). HPLC, Rt: 2.49 min. (purity 98.0%). LC/MS, M+(ESI): 350.9, M−(ESI): 348.9.
後処理
- customthe precipitate obtained
- filtrationwas filtered
- washwashed with water, Et2O, Acetonitrile
- customdried under vacuum at 40° C.
出典と根拠
- ORDレコード
- ord-55994a2eb7d04a519fd33c1d1c6ec273
- 出典データセット
- uspto-grants-2012_09
- 特許番号
- US08263595B2
反応ノート
読み込み中…