4-Butoxybenzoyl chloride → 4-Butoxy-N-[4'-(2,4-dioxothiazolidin-5-ylmethyl)-biphenyl-3-ylmethyl]-N-methylbenzamide
반응식
[CH3:1][NH:2][CH2:3][C:4]1[CH:5]=[C:6]([C:10]2[CH:15]=[CH:14][C:13]([CH2:16][CH:17]3[S:21][C:20](=[O:22])[NH:19][C:18]3=[O:23])=[CH:12][CH:11]=2)[CH:7]=[CH:8][CH:9]=1.[CH2:24]([O:28][C:29]1[CH:37]=[CH:36][C:32]([C:33](Cl)=[O:34])=[CH:31][CH:30]=1)[CH2:25][CH2:26][CH3:27]>>[CH2:24]([O:28][C:29]1[CH:37]=[CH:36][C:32]([C:33]([N:2]([CH2:3][C:4]2[CH:5]=[C:6]([C:10]3[CH:11]=[CH:12][C:13]([CH2:16][CH:17]4[S:21][C:20](=[O:22])[NH:19][C:18]4=[O:23])=[CH:14][CH:15]=3)[CH:7]=[CH:8][CH:9]=2)[CH3:1])=[O:34])=[CH:31][CH:30]=1)[CH2:25][CH2:26][CH3:27]참가 물질
3
실험 절차
In a manner similar to that of Example 37(e), by reacting 500 mg (1.5 mmol) of 5-(3′-methylaminomethylbiphenyl-4-ylmethyl)thiazolidine-2,4-dione with 290 μl (1.5 mmol) of 4-butoxybenzoyl chloride, and after purification, 550 mg (83%) of 4-20 butoxy-N-[4′-(2,4-dioxothiazolidin-5-ylmethyl)biphenyl-3-ylmethyl]-N-methylbenzamide are obtained in the form of a white solid with a melting point of 116° C.
후처리
- customafter purification, 550 mg (83%) of 4-20 butoxy-N-[4′-(2,4-dioxothiazolidin-5-ylmethyl)biphenyl-3-ylmethyl]-N-methylbenzamide
- customare obtained in the form of a white solid with a melting point of 116° C.
출처 및 근거
- ORD 기록
- ord-3e8882921a9f4376ad27e3d7cb0e5661
- 출처 데이터셋
- uspto-grants-2005_08
- 특허 번호
- US06927228B2
반응 노트
불러오는 중…