Water → HCID 136146567, 화합물
반응식
[F:1][C:2]1[C:11]([O:12][CH3:13])=[CH:10][CH:9]=[C:8]([F:14])[C:3]=1[C:4]([NH:6][OH:7])=[NH:5].C(N(CC)CC)C.Cl[C:23](OC1C=CC=CC=1)=[O:24].O>C(Cl)Cl.C1(C)C=CC=CC=1>[F:1][C:2]1[C:11]([O:12][CH3:13])=[CH:10][CH:9]=[C:8]([F:14])[C:3]=1[C:4]1[NH:5][C:23](=[O:24])[O:7][N:6]=1참가 물질
실험 절차
To an ice cold solution of 2,6-difluoro-N-hydroxy-3-methoxybenzamidine in DCM (5 ml) was added triethyl amine (0.07 g, 0.11 ml, 0.77 mmol) followed by dropwise addition of phenyl chloroformate. The resulting reaction mixture was stirred at room temperature for 1 h. After the completion of the reaction (TLC monitoring), the organic layer was washed with water until the DCM layer was neutral. The organic layer was dried (Na2SO4), filtered and concentrated to get a white solid. The solid compound was then dissolved in toluene (2 ml) and refluxed it at 100° C. for 2 h. After the completion of the reaction (TLC monitoring), water (100 ml) was added and extracted with ethyl acetate (3×100 ml). The combined organics was washed with water, brine, dried (Na2SO4), filtered and concentrated. The crude residue was purified over silica gel (60-120 M, 35% EtOAc-Hexane) to get the desired product (0.09 g, 80%) as a white solid. MS ES+ (229.18).
후처리
- customThe resulting reaction mixture
- customAfter the completion of the reaction (TLC monitoring)
- washthe organic layer was washed with water until the DCM layer
- dry with materialThe organic layer was dried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated
- customto get a white solid
- temperaturerefluxed it at 100° C. for 2 h
- additionwas added
- extractionextracted with ethyl acetate (3×100 ml)
- washThe combined organics was washed with water, brine
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated
- customThe crude residue was purified over silica gel (60-120 M, 35% EtOAc-Hexane)
출처 및 근거
- ORD 기록
- ord-78f7af9bcebb4839b8860794eb346d73
- 출처 데이터셋
- uspto-grants-2013_04
- 특허 번호
- US08415383B2
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