반응식
[CH3:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([NH2:9])=[C:4]([NH2:10])[CH:3]=1.[N+]([C:14]1[CH:15]=[C:16]([C:21]([F:24])([F:23])[F:22])[CH:17]=[CH:18][C:19]=1Br)([O-])=O.NC1C(N)=C(NC2C=CC=CC=2)C=CC=1>Cl>[CH3:8][C:7]1[C:2]([CH3:1])=[CH:3][C:4]2[C:5](=[N:9][C:19]3[C:18]([N:10]=2)=[CH:17][C:16]([C:21]([F:24])([F:23])[F:22])=[CH:15][CH:14]=3)[CH:6]=1참가 물질
5
실험 절차
The 2,3-dimethyl-7-trifluoromethylphenazine was prepared in a 3-step process, starting with 4,5-dimethyl-1,2-phenylenediamine and 3-nitro-4-bromobenzotrifluoride. The nucleophilic substitution product being the biarylamine was then reduced with stannous chloride in conc. HCl to the diamino diphenylamine.
출처 및 근거
- ORD 기록
- ord-90f75670a9244c1c83e6ad561753cf71
- 출처 데이터셋
- uspto-grants-2000_02
- 특허 번호
- US06020987
연결된 노트
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