반응식
[CH2:1]([O:3][C:4](=[O:8])[CH2:5][CH2:6][NH2:7])[CH3:2].CCN(CC)CC.[Cl:16][C:17]1[CH:18]=[C:19]([NH:23][C:24]2[O:25][C:26]([C:29]3[CH:34]=[CH:33][C:32]([CH:35]4[CH2:40][CH2:39][CH:38]([CH2:41][C:42](O)=[O:43])[CH2:37][CH2:36]4)=[CH:31][CH:30]=3)=[CH:27][N:28]=2)[CH:20]=[CH:21][CH:22]=1.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C>CN(C=O)C.CCOC(C)=O.O>[CH2:1]([O:3][C:4](=[O:8])[CH2:5][CH2:6][NH:7][C:42](=[O:43])[CH2:41][CH:38]1[CH2:37][CH2:36][CH:35]([C:32]2[CH:31]=[CH:30][C:29]([C:26]3[O:25][C:24]([NH:23][C:19]4[CH:20]=[CH:21][CH:22]=[C:17]([Cl:16])[CH:18]=4)=[N:28][CH:27]=3)=[CH:34][CH:33]=2)[CH2:40][CH2:39]1)[CH3:2]참가 물질
반응물 5
생성물 1
시약·촉매·용매 3
실험 절차
To a solution of 3-aminopropionic acid ethyl ester (41 mg, 0.268 mmol) and Et3N (0.082 mL, 0.730 mmol) is added a solution of (4-{4-[2-(3-Chlorophenylamino)-oxazol-5-yl]-phenyl}-cyclohexyl)-acetic acid (100 mg, 0.243 mmol) in DMF (4 mL), HATU (102 mg, 0.268 mmol) and iPr2NEt (0.127 mL, 0.73 mmol). The reaction mixture is allowed to stir at ambient temperature for 18 h. Water is added and EtOAc is used to extract. The organic layer is washed with brine, dried with Na2SO4 and concentrated to give the title compound (140 mg) as a tan solid: 1H NMR (400 MHz, DMSO-d6) δ ppm 1.02-1.13 (m, 2H) 1.18 (t, J=7.07 Hz, 3H) 1.38-1.50 (m, 2H) 1.71 (dd, J=7.71, 4.17 Hz, 1H) 1.78 (t, J=12.63 Hz, 4H) 1.98 (d, J=6.57 Hz, 2H) 2.44 (t, J=6.82 Hz, 2H) 3.25-3.28 (m, 2H) 4.06 (q, J=7.07 Hz, 2H) 6.99 (ddd, J=7.89, 1.96, 1.01 Hz, 1H) 7.27-7.35 (m, 1H) 7.29 (d, J=8.59 Hz, 2H) 7.40 (s, 1H) 7.50 (d, J=8.34 Hz, 1H) 7.47-7.52 (m, 1H) 7.85 (t, J=2.02 Hz, 1H) 7.88 (t, J=5.81 Hz, 1H) 10.52 (s, 1H); (M+H)+510.2.
후처리
- extractionto extract
- washThe organic layer is washed with brine
- dry with materialdried with Na2SO4
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-c53c386839574ef6b0686e9f992c0bb2
- 출처 데이터셋
- uspto-grants-2014_09
- 특허 번호
- US08835451B2
연결된 노트
불러오는 중…