반응식
[C:1]([C:5]1[CH:13]=[CH:12][C:8]([C:9](=[S:11])[NH2:10])=[CH:7][CH:6]=1)([O:3][CH3:4])=[O:2].Cl[CH2:15][C:16]([C:18]1[CH:19]=[C:20]2[C:25](=[CH:26][CH:27]=1)[C:24]([CH3:29])([CH3:28])[CH2:23][CH2:22][C:21]2([CH3:31])[CH3:30])=O.O>C(O)(C)C.N1C=CC=CC=1>[C:1]([C:5]1[CH:13]=[CH:12][C:8]([C:9]2[S:11][CH:15]=[C:16]([C:18]3[CH:27]=[CH:26][C:25]4[C:24]([CH3:29])([CH3:28])[CH2:23][CH2:22][C:21]([CH3:31])([CH3:30])[C:20]=4[CH:19]=3)[N:10]=2)=[CH:7][CH:6]=1)([O:3][CH3:4])=[O:2]참가 물질
6
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
3.2 g (16.5 moles) of 4-carbomethoxybenzothiamide and 4.2 g (16 millimoles) of 6-chloroacetyl-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene (for preparation see Example 28) in 40 ml of isopropanol were refluxed for 1 hour with the addition of 2 drops of pyridine. The mixture was cooled, water was added and the crystals formed were filtered off under suction. Recrystallization from isopropanol and a trace of water gave 3.0 g the title compound of melting point 138°-140° C.
후처리
- temperatureThe mixture was cooled
- customthe crystals formed
- filtrationwere filtered off under suction
- customRecrystallization from isopropanol
출처 및 근거
- ORD 기록
- ord-9e45ef78e54041aba77d1d2fdd700bd3
- 출처 데이터셋
- uspto-grants-1993_04
- 특허 번호
- US05206242
연결된 노트
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