반응식
CCN=C=NCCCN(C)C.Cl.[C:13]([O:16][C:17]1[CH:25]=[CH:24][C:23]([Cl:26])=[CH:22][C:18]=1[C:19]([OH:21])=O)(=[O:15])[CH3:14].Cl.[NH2:28][CH2:29][C:30]([NH:32][C:33]1[CH:38]=[C:37]([C:39]([F:42])([F:41])[F:40])[CH:36]=[C:35]([C:43]([F:46])([F:45])[F:44])[CH:34]=1)=[O:31].ON1C2C=CC=CC=2N=N1.Cl>CN(C)C=O>[C:13]([O:16][C:17]1[CH:25]=[CH:24][C:23]([Cl:26])=[CH:22][C:18]=1[C:19]([NH:28][CH2:29][C:30](=[O:31])[NH:32][C:33]1[CH:38]=[C:37]([C:39]([F:42])([F:41])[F:40])[CH:36]=[C:35]([C:43]([F:44])([F:45])[F:46])[CH:34]=1)=[O:21])(=[O:15])[CH3:14]참가 물질
반응물 5
생성물 1
시약·촉매·용매 1
실험 절차
WSC.HCl (95.9 mg, 0.5 mmol) was added to a solution of 2-acetoxy-5-chlorobenzoic acid (59.1 mg, 0.28 mmol), 2-amino-N-[3,5-bis(trifluoromethyl)phenyl]acetamide hydrochloride (80.8 mg, 0.25 mmol) and 1-hydroxybenzotriazole (37.2 mg, 0.28 mmol) in N,N-dimethylformamide (3 mL), and the mixture was stirred at room temperature for 3 hours. The reaction mixture was poured into diluted hydrochloric acid and extracted with ethyl acetate. After the ethyl acetate layer was washed with brine, dried over anhydrous sodium sulfate, the residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=3:2→1:1) to give the title compound (83.7 mg, 69.3%) as a white crystal.
후처리
- extractionextracted with ethyl acetate
- washAfter the ethyl acetate layer was washed with brine
- dry with materialdried over anhydrous sodium sulfate
- customthe residue obtained by evaporation of the solvent under reduced pressure
- customwas purified by column chromatography on silica gel (n-hexane:ethyl acetate=3:2→1:1)
출처 및 근거
- ORD 기록
- ord-ebf4a2408dec4108a5d720d6086f8553
- 출처 데이터셋
- uspto-grants-2010_04
- 특허 번호
- US07700655B2
연결된 노트
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