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[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.[C:15]1([CH3:25])[CH:20]=[CH:19][C:18]([S:21](Cl)(=[O:23])=[O:22])=[CH:17][CH:16]=1.C(OCC)(=O)C.CCCCCC>C(Cl)Cl.CCOCC>[C:2]1([NH:1][S:21]([C:18]2[CH:19]=[CH:20][C:15]([CH3:25])=[CH:16][CH:17]=2)(=[O:23])=[O:22])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1참가 물질
실험 절차
Aniline (1.86 g, 0.02 mol) was dissolved in methylene chloride under nitrogen and triethylamine (3.8 mL, 0.02 mol) was added. This solution wascooled in an ice bath and a solution of p-toluenesulfonyl chloride (3.8 g, 0.02 mol) was added dropwise via a syringe. After stirring this solution for 4 h at room temperature, TLC analysis (silica gel, 20% ethyl acetate/hexane) indicated completion of the reaction. The reaction mixturewas poured into ether and the precipitate filtered. The ether layer was washed with water, dried over MgSO4 and concentrated to yield an oilymaterial. This crude product was chromatographed on silica using 35% ethyl acetate and hexane to obtain a solid which was further recrystallized in methylene chloride/hexane; m.p. 104° C.; 1H NMR (CDCl3) δ2.36 (s, 3H), 7.07-7.25 (m, 8H), 7.67-7.69 (d, 2H).
후처리
- customThis solution wascooled in an ice bath
- customcompletion of the reaction
- filtrationthe precipitate filtered
- washThe ether layer was washed with water
- dry with materialdried over MgSO4
- concentrationconcentrated
- customto yield an oilymaterial
- customThis crude product was chromatographed on silica using 35% ethyl acetate and hexane
- customto obtain a solid which
- customwas further recrystallized in methylene chloride/hexane
출처 및 근거
- ORD 기록
- ord-c252f627c2fd4c92ac36b2911bd08852
- 출처 데이터셋
- uspto-grants-1996_02
- 특허 번호
- US05491072
연결된 노트
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