2,3-Dichloronitrobenzene → (7-Chloro-1H-benzimidazol-1-yl)acetic acid
반응식
Br[C:2]1[C:7]2[N:8]([CH2:11][C:12]([OH:14])=[O:13])[CH:9]=[N:10][C:6]=2[CH:5]=[CH:4][CH:3]=1.[Cl:15]C1C=CC=C([N+]([O-])=O)C=1Cl>>[Cl:15][C:2]1[C:7]2[N:8]([CH2:11][C:12]([OH:14])=[O:13])[CH:9]=[N:10][C:6]=2[CH:5]=[CH:4][CH:3]=1참가 물질
3
실험 절차
Alternatively, the title compound was synthesised according to the procedure described for the synthesis of (7-bromo-1H-benzimidazol-1-yl)acetic acid (parts A-D) starting from 1,2-dichloro-3-nitrobenzene. The new intermediates isolated were:
후처리
- customThe new intermediates isolated
출처 및 근거
- ORD 기록
- ord-432688e682954a388ee3920837737f30
- 출처 데이터셋
- uspto-grants-2010_01
- 특허 번호
- US07645784B2
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