Hydrochloric Acid → 2-oxo-3-(2-pyridinyl)-1-Imidazolidineacetic acid
反応式
[O:1]=[C:2]1[N:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=2)[CH2:5][CH2:4][N:3]1[CH2:13][C:14]([O:16]C(C)(C)C)=[O:15].Cl>CCOC(C)=O>[O:1]=[C:2]1[N:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=2)[CH2:5][CH2:4][N:3]1[CH2:13][C:14]([OH:16])=[O:15]参加物
4
実験手順
A solution of tert-butyl (2-oxo-3-pyridin-2-ylimidazolidin-1-yl)acetate from Step B (150 mg, 0.54 mmol) in EtOAc (10 mL) at 0° C. was saturated with HCl (g). The mixture was stood at 0° C. for a total of 30 min, then concentrated in vacuo to give the title compound. MS: m/z=222 (M+1).
後処理
- customat 0° C.
- customwas stood at 0° C. for a total of 30 min
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-e9fff566f67649e29828082ec7b7ce07
- 出典データセット
- uspto-grants-2010_02
- 特許番号
- US07659300B2
反応ノート
読み込み中…