Hydrochloric Acid → Ethyl (5-ethoxypyrazin-2-yl)carbamate
反応式
Cl[C:2]1[N:3]=[CH:4][C:5]([NH:8][C:9](=[O:15])[O:10][C:11]([CH3:14])(C)C)=[N:6][CH:7]=1.Cl.[CH3:17][CH2:18][O:19]C(C)=O>[O-]CC.[Na+]>[CH2:18]([O:19][C:2]1[N:3]=[CH:4][C:5]([NH:8][C:9](=[O:15])[O:10][CH2:11][CH3:14])=[N:6][CH:7]=1)[CH3:17]参加物
5
実験手順
The mixed products from 1,1-dimethylethyl (5-chloro-2-pyrazinyl)carbamate were combined and refluxed in 24% sodium ethoxide for 5 days, then cooled to RT, neutralized with HCl, and the product extracted out with DCM. The DCM was washed with saturated NaHCO3, then concentrated to afford a black residue. Addition of EtOAc afforded solids that were filtered off, washed with EtOAc to give ethyl (5-ethoxypyrazin-2-yl)carbamate as a brown solid (3.5 g, 42.9%).
後処理
- extractionthe product extracted out with DCM
- washThe DCM was washed with saturated NaHCO3
- concentrationconcentrated
- customto afford a black residue
- filtrationwere filtered off
- washwashed with EtOAc
出典と根拠
- ORDレコード
- ord-66e5bca0997f495689b182c904655b6b
- 出典データセット
- uspto-grants-2015_11
- 特許番号
- US09187464B2
反応ノート
読み込み中…