N-methanesulfonyl-6-bromomethylindole → (3-Chloro-4-methyl-5-nitrophenyl) acetonitrile
반응식
Br[CH2:2][C:3]1[CH:4]=[C:5]([N+:11]([O-:13])=[O:12])[C:6]([CH3:10])=[C:7]([Cl:9])[CH:8]=1.CS([N:18]1C2C(=CC=C(CC#N)C=2)C=[CH:19]1)(=O)=O.CS(N1C2C(=CC=C(CBr)C=2)C=C1)(=O)=O>>[Cl:9][C:7]1[CH:8]=[C:3]([CH2:2][C:19]#[N:18])[CH:4]=[C:5]([N+:11]([O-:13])=[O:12])[C:6]=1[CH3:10]참가 물질
4
실험 절차
(3-Chloro-4-methyl-5-nitrophenyl) acetonitrile was prepared from 5-bromomethyl-1-chloro-2-methyl-3-nitrobenzene in a manner similar to that described in Example 10 for the preparation of N-methanesulfonyl-6-cyanomethyl indole from N-methanesulfonyl-6-bromomethyl indole.
출처 및 근거
- ORD 기록
- ord-fdab174fc2dc49d79a2f83186a21f4f9
- 출처 데이터셋
- uspto-grants-2000_05
- 특허 번호
- US06057349
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