反応式
Cl.[C:2](N)(=[NH:5])[CH2:3][CH3:4].[CH3:7][O:8][C:9]1[CH:18]=[CH:17][C:12]([C:13]([NH:15][NH2:16])=[O:14])=[CH:11][CH:10]=1>>[NH:5]=[C:2]([N:15]([C:13](=[O:14])[C:12]1[CH:11]=[CH:10][C:9]([O:8][CH3:7])=[CH:18][CH:17]=1)[NH2:16])[CH2:3][CH3:4]参加物
3
実験手順
Prepared from 4.90 g (45 mmol) propioamidine hydrochloride and 5.00 g (30 mmol) 4-methoxy-benzoic acid hydrazide analogously to the procedure laid down for intermediate product 1a). After distillation of the ethanol 10.0 g crude product are obtained, which are reacted without any further purification.
後処理
- distillationAfter distillation of the ethanol 10.0 g crude product
- customare obtained
- customwhich are reacted without any further purification
出典と根拠
- ORDレコード
- ord-11be8ab7e1c64170894019d1b1ce419a
- 出典データセット
- uspto-grants-2008_09
- 特許番号
- US07423036B2
関連ノート
読み込み中…