Cyclohexanecarbonyl chloride → Benzimidazole
반응식
NC1C=CC([C:8]2[NH:9][C:10]3[CH:16]=[CH:15][C:14](N)=[CH:13][C:11]=3[N:12]=2)=CC=1.C1(C(Cl)=O)CCCCC1>>[N:9]1[C:10]2[CH:16]=[CH:15][CH:14]=[CH:13][C:11]=2[NH:12][CH:8]=1참가 물질
3
실험 절차
2-(N-Cyclohexylcarbonyl-4′-aminophenyl)-6-cyclohexylcarbonylamino)-benzimidazole was prepared by Method A from 2-(4-aminophenyl)-6-aminobenzimidazole (0.195 g, 0.87 mmole) and cyclohexylcarbonyl chloride (0.291 ml, 0.319 g, 2.175 mmole). The resulting solid (76.7 mg) was purified by preparative HPLC.
후처리
- customThe resulting solid (76.7 mg) was purified by preparative HPLC
출처 및 근거
- ORD 기록
- ord-846edf29646848ffb9b26b83d99d7e9d
- 출처 데이터셋
- uspto-grants-2005_06
- 특허 번호
- US06911462B2
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