반응식
C(P(CCCC)CCCC)CCC.[CH3:14][C:15]1[C:20]([CH2:21][OH:22])=[CH:19][CH:18]=[C:17]([C:23]([F:26])([F:25])[F:24])[N:16]=1.[CH3:27][O:28][C:29](=[O:43])[CH2:30][C:31]1[C:35]2[C:36]([CH3:42])=[CH:37][C:38](O)=[C:39]([CH3:40])[C:34]=2[S:33][CH:32]=1.C1CCN(C(N=NC(N2CCCCC2)=O)=O)CC1>C1COCC1>[CH3:27][O:28][C:29](=[O:43])[CH2:30][C:31]1[C:35]2[C:36]([CH3:42])=[CH:37][C:38]([O:22][CH2:21][C:20]3[C:15]([CH3:14])=[N:16][C:17]([C:23]([F:24])([F:26])[F:25])=[CH:18][CH:19]=3)=[C:39]([CH3:40])[C:34]=2[S:33][CH:32]=1참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
To a mixture of tri-n-butylphosphine (0.196 mL), (2-methyl-6-(trifluoromethyl)pyridin-3-yl)methanol (105 mg), methyl(6-hydroxy-4,7-dimethyl-1-benzothiophen-3-yl)acetate (130.9 mg) and THF (5.0 mL) was added ADDP (198 mg) at room temperature. The mixture was stirred at room temperature overnight under nitrogen atmosphere. The mixture was concentrated in vacuo. To the residue was added IPE, and the precipitate was filtered off. The filtrate was concentrated in vacuo. The residue was purified by silica gel column chromatography (EtOAc/hexane) to give the title compound (159 mg) as solid. The solid was crystallized from EtOAc-hexane.
후처리
- concentrationThe mixture was concentrated in vacuo
- additionTo the residue was added IPE
- filtrationthe precipitate was filtered off
- concentrationThe filtrate was concentrated in vacuo
- customThe residue was purified by silica gel column chromatography (EtOAc/hexane)
출처 및 근거
- ORD 기록
- ord-6ee8ad386e8b49789e726bac523dd442
- 출처 데이터셋
- uspto-grants-2016_01
- 특허 번호
- US09238639B2
연결된 노트
불러오는 중…