반응식
[C:1]([C:4]1[C:5]([F:21])=[C:6]([F:20])[C:7]([N:12]2[CH2:17][C@H:16]([CH3:18])[O:15][C@H:14]([CH3:19])[CH2:13]2)=[C:8]([CH:11]=1)[CH:9]=O)(=[O:3])[CH3:2].[NH:22]1[C:29](=[O:30])[CH2:28][C:26](=[O:27])[NH:25][C:23]1=[O:24]>CC(O)C>[C:1]([C:4]1[CH:11]=[C:8]2[C:7](=[C:6]([F:20])[C:5]=1[F:21])[N:12]1[CH2:17][C@@H:16]([CH3:18])[O:15][C@@H:14]([CH3:19])[C@@H:13]1[C:28]1([C:26](=[O:27])[NH:25][C:23](=[O:24])[NH:22][C:29]1=[O:30])[CH2:9]2)(=[O:3])[CH3:2]참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 85 °C
실험 절차
To a solution of 5-acetyl-2-((2R,6S)-2,6-dimethyl-morpholin-4-yl)-3,4-difluoro-benzaldehyde (Intermediate 11, 3.0 g, 9.17 mmol) in IPA was added barbituric acid (1.4 g, 11.00 mmol), and the mixture was heated at 85° C. for 12 hours. Solvents were evaporated and the residue was purified over neutral alumina using a gradient of methanol in CH2Cl2 to give the title compound as a racemic mixture in the form of an off-white solid. Yield: 3.0 g (75%).
후처리
- customSolvents were evaporated
- customthe residue was purified over neutral alumina using a gradient of methanol in CH2Cl2
출처 및 근거
- ORD 기록
- ord-3a2ef7a8c82541e096659b691eb6fea3
- 출처 데이터셋
- uspto-grants-2014_02
- 특허 번호
- US08658641B2
연결된 노트
불러오는 중…