반응식
[C:1]([O:5][C:6]([NH:8][C@@H:9]([CH:13]1[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1)[C:10]([OH:12])=O)=[O:7])([CH3:4])([CH3:3])[CH3:2].CN(C(ON1N=N[C:29]2[CH:30]=[CH:31][CH:32]=[CH:33][C:28]1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C1C=CC2[N:51](O)[N:50]=[N:49][C:47]=2C=1.[CH:53]([N:56]([CH:59]([CH3:61])[CH3:60])CC)([CH3:55])C.CC([N:65](C)C)=O>C(Cl)Cl>[C:1]([O:5][C:6](=[O:7])[NH:8][CH:9]([CH:13]1[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1)[C:10]([N:56]1[CH2:53][CH2:55][CH2:61][C@H:59]1[C:60]1[N:51]=[N:50][N:49]([CH2:47][C:28]2[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=2)[N:65]=1)=[O:12])([CH3:2])([CH3:3])[CH3:4]참가 물질
반응물 5
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of (S)-tert-butoxycarbonylamino-cyclohexyl-acetic acid (123.8 mg, 0.48 mmol) in DMA (5 mL) is added HBTU (248.8 mg, 0.656 mmol), HOBt (88.6 mg, 0.656 mmol) and diisopropylethylamine (305 uL, 1.75 mmol). The mixture is stirred at room temperature for 5 minutes. A solution of compound D in DCM (5 mL) is added to the above mixture at 0° C. The reaction mixture is stirred at room temperature for 1 hour and concentrated under vacuum. The residue is diluted with EtOAc. The organic is washed with brine, citric acid (5%), brine, NaHCO3 (Sat.) and brine. The organic layer is then dried and concentrated under vacuum. The residue is purified by flash column chromatography (Hexanes/EtOAc) to provide the title compound 190 mg (92%). M+H+=369.
후처리
- stirringThe reaction mixture is stirred at room temperature for 1 hour
- concentrationconcentrated under vacuum
- additionThe residue is diluted with EtOAc
- washThe organic is washed with brine, citric acid (5%), brine, NaHCO3 (Sat.) and brine
- customThe organic layer is then dried
- concentrationconcentrated under vacuum
- customThe residue is purified by flash column chromatography (Hexanes/EtOAc)
출처 및 근거
- ORD 기록
- ord-7709b56c7bfe46e192362c88c5d88a45
- 출처 데이터셋
- uspto-grants-2012_06
- 특허 번호
- US08207183B2
연결된 노트
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