Ammonium Hydroxide → 5-(6-Aminopyridin-3-yl)piperidin-2-one
反応式
F[C:2]1[N:7]=[CH:6][C:5]([CH:8]2[CH2:13][CH2:12][CH2:11][N:10](COCC[Si](C)(C)C)[C:9]2=O)=[CH:4][CH:3]=1.[OH-:23].[NH4+:24]>CO.C1(C)C=CC=CC=1>[NH2:24][C:2]1[N:7]=[CH:6][C:5]([CH:8]2[CH2:9][NH:10][C:11](=[O:23])[CH2:12][CH2:13]2)=[CH:4][CH:3]=1参加物
5
実験手順
To -(6-fluoropyridin-3-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)piperidin-2-one (290 mg, 0.894 mmol) in a steel bomb, ammonium hydroxide (34.8 μl, 0.894 mmol) solution was added (40% head volume remained). The steel bomb reactor was heated at 150° C. for 44 h (250 psi on pressure gauge). LCMS—0.23 min, MH+192.1 (without SEM); 0.66 min, MH+322.1 (with SEM). After diluted with MeOH and toluene, volatile materials were completely removed in vacuo. 5-(6-aminopyridin-3-yl)piperidin-2-one was used for the next step.
後処理
- customLCMS—0.23 min, MH
- custom0.66 min, MH
- customwere completely removed in vacuo
出典と根拠
- ORDレコード
- ord-ab11cc6df8af47e69d2cc0cfc725a106
- 出典データセット
- uspto-grants-2016_01
- 特許番号
- US09242996B2
反応ノート
読み込み中…