반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([OH:11])[CH:10]=1)[C:5](O)=[O:6].Cl.C[N:14](C)CCCN=C=NCC.O.ON1C2C=CC=CC=2N=N1.CCN(CC)CC>C(Cl)Cl.CCOC(C)=O.CN(C=O)C>[OH:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([OH:11])[CH:10]=1)[C:5]([NH2:14])=[O:6]참가 물질
반응물 4
생성물 1
시약·촉매·용매 3
실험 절차
After reaction step (a), the resulting amine (1 equiv.), 3,5-dihydroxybenzoic acid (1 equiv.), EDCI (1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride) (1.2 equiv.), HOBt (1-hydroxybenzotriazole hydrate) (1.2 equiv.), and Et3N (4 equiv.) in CH2Cl2.DMF (9:1) were stirred for 12 hours at room temperature. Then the reaction mixture was diluted with EtOAc and the organic layer washed with brine. The combined organic layer was dried over anhydrous Na2SO4 and concentrated. Purification of the resulting crude product by flash silica gel chromatography provided corresponding 3,5-dihydroxybenzamide derivative. The above derivative (1 equiv.) and active carbonate 4 (1.1 equiv.) in THF were stirred under hydrogen atmosphere in presence of Pd—C (10%) for 12 hours at room temperature. Then the reaction mixture was filtered and the organic layer washed with brine. The combined organic layer was dried over anhydrous Na2SO4 and concentrated. Purification of the resulting crude product by flash silica gel chromatography provided compound 134 as a solid.
후처리
- customAfter reaction step (a)
- washthe organic layer washed with brine
- dry with materialThe combined organic layer was dried over anhydrous Na2SO4
- concentrationconcentrated
- customPurification of the resulting crude product by flash silica gel chromatography
출처 및 근거
- ORD 기록
- ord-7efcf994c2e943c1970d84ab2f92882f
- 출처 데이터셋
- uspto-grants-2011_03
- 특허 번호
- US07897635B2
연결된 노트
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