Acetic Anhydride → HCID 178474553、化合物
反応式
[NH2:1][CH2:2][C:3]1[CH:8]=[CH:7][C:6]([NH:9]/[C:10](=[C:17]2\[C:18](=[O:26])[NH:19][C:20]3[C:25]\2=[CH:24][CH:23]=[CH:22][CH:21]=3)/[C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:5][CH:4]=1.[C:27](OC(=O)C)(=[O:29])[CH3:28]>C(O)(=O)C>[C:27]([NH:1][CH2:2][C:3]1[CH:4]=[CH:5][C:6]([NH:9]/[C:10](=[C:17]2\[C:18](=[O:26])[NH:19][C:20]3[C:25]\2=[CH:24][CH:23]=[CH:22][CH:21]=3)/[C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:7][CH:8]=1)(=[O:29])[CH3:28]参加物
4
実験手順
Prepared analogously to Example 31 from (Z)-3-[1-(4-aminomethyl-phenylamino)-1-phenyl-methylidene]-2-indolinone, glacial acetic acid and acetic anhydride.
出典と根拠
- ORDレコード
- ord-33100f0b47014c7cab1d61bca4ede475
- 出典データセット
- uspto-grants-2005_02