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C(O[C@H]([C@H](C(O)=O)OC(=O)C1C=CC=CC=1)C(O)=O)(=O)C1C=CC=CC=1.[CH2:27]([C:29]1[CH:30]=[CH:31][C:32]([CH2:35][CH2:36][O:37][C:38]2[CH:51]=[CH:50][C:41]([CH2:42][C@H:43]3[S:47][C:46](=[O:48])[NH:45][C:44]3=[O:49])=[CH:40][CH:39]=2)=[N:33][CH:34]=1)[CH3:28].[ClH:52]>CO>[ClH:52].[CH2:27]([C:29]1[CH:30]=[CH:31][C:32]([CH2:35][CH2:36][O:37][C:38]2[CH:51]=[CH:50][C:41]([CH2:42][C@H:43]3[S:47][C:46](=[O:48])[NH:45][C:44]3=[O:49])=[CH:40][CH:39]=2)=[N:33][CH:34]=1)[CH3:28]참가 물질
실험 절차
The product from Example 15, Step 3 was dissolved in MeOH (2.25 mL) containing 37% HCl (0.134 mL) at 35° C. The solution was filtered, EtOAc (9 mL) was poured into the stirred solution and the mixture stirred for 20 min. The white solid was collected by filtration, washed with EtOAc and dried at 30° C. under high vacuum to give the title compound (0.181 g). (Method 1) 98.3%, Rt 10.65 min.; 1.7%, Rt 14.83 min e.e. 96.6%. LCMS (Method 2): Rt 2.90 min 99.39%, m/z 357 [MH+—HCl]. LCMS (Method 3) Rt 2.91 min, m/z 357 [MH+—HCl]. 1H NMR (400 MHz, DMSO-d6): δ 12.0 (1 H, s), 8.70 (1 H, d, J 1.7 Hz), 8.36 (1 H, bd, J 8.3 Hz), 7.93 (1 H, d, J 8.2 Hz), 7.15, 6.87 (4 H, A2B2q, J 8.7 Hz), 4.86 (1 H, dd, J 4.4, 8.9 Hz), 4.38 (2 H, t, J 6.3 Hz), 3.44 (2 H, t, J 6.2 Hz), 3.29 (1 H, dd, J 4.3, 14.2 Hz), 3.06 (1 H, dd, J 9.0, 14.3 Hz), 2.78 (2 H, q, J 7.6 Hz), 1.23 (3 H, t, J 7.6 Hz).
후처리
- filtrationThe solution was filtered
- additionEtOAc (9 mL) was poured into the stirred solution
- filtrationThe white solid was collected by filtration
- washwashed with EtOAc
- customdried at 30° C. under high vacuum
출처 및 근거
- ORD 기록
- ord-c833079e1ef0408eba2c076a364e5330
- 출처 데이터셋
- uspto-grants-2014_08
- 특허 번호
- US08815837B2
연결된 노트
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