反応式
Br[CH2:2][C:3]1[C:11]2[N:10]=[CH:9]N(C(OC(C)(C)C)=O)[C:7]=2[CH:6]=[CH:5][CH:4]=1.[CH3:19][N:20]([CH:22]([C:28](OCC)=O)[C:23](OCC)=O)[CH3:21].C(N(C(C(OCC)=O)C(OCC)=O)CCC)CC>>[CH3:19][N:20]([CH3:21])[CH:22]1[CH2:28][C:7]2[C:11]3=[C:3]([CH2:2][CH2:9][N:10]3[CH2:23]1)[CH:4]=[CH:5][CH:6]=2参加物
4
実験手順
This compound was prepared by following the procedure of Example 18, but substituting t-butyl 2,3-dihydro-7-(bromomethyl)-1H-indole-1-carboxylate for t-butyl 4-(bromomethyl)-1H-benzimidazole-1-carboxylate and diethyl (dimethylamino)malonate for diethyl (dipropylamino)malonate.
後処理
- customThis compound was prepared
出典と根拠
- ORDレコード
- ord-bf8491db5dc44eb6b5efc91bcb32be1d
- 出典データセット
- uspto-grants-1995_07
- 特許番号
- US05436240
関連ノート
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