Guanidine → 2-Amino-10-bromo-5H,7H-benzo[b]pyrimido[4,5-d]azepin-6-one
反応式
[Br:1][C:2]1[CH:18]=[CH:17][C:5]2[NH:6][C:7](=[O:16])[CH2:8][C:9](=[CH:12]N(C)C)[C:10](=O)[C:4]=2[CH:3]=1.[NH2:19][C:20]([NH2:22])=[NH:21]>>[NH2:21][C:20]1[N:22]=[CH:12][C:9]2[CH2:8][C:7](=[O:16])[NH:6][C:5]3[CH:17]=[CH:18][C:2]([Br:1])=[CH:3][C:4]=3[C:10]=2[N:19]=1参加物
3
実験手順
In a manner similar to that described in method H, 7-bromo-4-dimethylaminomethylene-3,4-dihydro-1H-benzo[b]azepine-2,5-dione (v-k) and guanidine were converted to I-44 (79%): HRMS Calcd. for C12H9BrN4O: 305.0037, Found 305.0042.
出典と根拠
- ORDレコード
- ord-667d67962a2b48f1a89f0c5681b5649a
- 出典データセット
- uspto-grants-2011_05
- 特許番号
- US07935694B2
反応ノート
読み込み中…