반응식
FC(F)(F)C(O)=O.C([O:12][CH2:13][CH:14]([C:25]1[N:34]([C:35]2[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=2)[C:33](=[O:41])[C:32]2[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=2)[N:26]=1)[NH:15][C:16]1[N:24]=[CH:23][N:22]=[C:21]2[C:17]=1[N:18]=[CH:19][NH:20]2)(C)(C)C>ClCCl>[OH:12][CH2:13][CH:14]([C:25]1[N:34]([C:35]2[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=2)[C:33](=[O:41])[C:32]2[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=2)[N:26]=1)[NH:15][C:16]1[N:24]=[CH:23][N:22]=[C:21]2[C:17]=1[N:18]=[CH:19][NH:20]2참가 물질
4
실험 절차
Compound 92 was prepared by adding trifluoroacetic acid to a solution of 2-[2-tert-butoxy-1-(9H-purin-6-ylamino)-ethyl]-3-phenyl-3H-quinazolin-4-one in dichloromethane. The reaction was stirred at ambient temperature for 18 hours, then concentrated in vacuo. Purification by LC provided the product as a white solid. MS (ES): m/z 400 (M H), 382, 200, 136. Compound 92 is shown below.
후처리
- concentrationconcentrated in vacuo
- customPurification by LC
출처 및 근거
- ORD 기록
- ord-a5b62c916f354d34adf9b20cbef2f4fc
- 출처 데이터셋
- uspto-grants-2014_07
- 특허 번호
- US08779131B2
연결된 노트
불러오는 중…