Hydrochloric Acid → 4-hydroxy-5-methyl-6-(2-(methylamino)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-7-yl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid hydrochloride
반응식
C([O:8][C:9]1[N:24]=[C:23]([C:25]2[CH:33]=[CH:32][C:31]3[N:30]4[CH2:34][CH:35]([NH:37][CH3:38])[CH2:36][C:29]4=[CH:28][C:27]=3[CH:26]=2)[C:22]([CH3:39])=[C:21]([O:40]CC2C=CC=CC=2)[C:10]=1[C:11]([O:13]CC1C=CC=CC=1)=[O:12])C1C=CC=CC=1.[ClH:48]>CO.[Pd]>[ClH:48].[OH:40][C:21]1[C:22]([CH3:39])=[C:23]([C:25]2[CH:33]=[CH:32][C:31]3[N:30]4[CH2:34][CH:35]([NH:37][CH3:38])[CH2:36][C:29]4=[CH:28][C:27]=3[CH:26]=2)[NH:24][C:9](=[O:8])[C:10]=1[C:11]([OH:13])=[O:12]참가 물질
5
반응물 2
생성물 1
시약·촉매·용매 2
실험 절차
The intermediate from Step 2 (70 mg, 0.11 mmol) was dissolved in MeOH (2 mL). To the solution was added 10% Pd/C (20 mg) and 3 N HCl in MeOH (0.1 mL). The mixture was stirred under H2 (1 atm) at room temperature for 16 h. The mixture was filtered through a 5 μm cartridge. The filtrate was concentrated, leaving the product (21 mg, 49%) as an off white powder.
후처리
- filtrationThe mixture was filtered through a 5 μm cartridge
- concentrationThe filtrate was concentrated
출처 및 근거
- ORD 기록
- ord-c9ba8f07d29d4c1aa39698fe1e2d0d62
- 출처 데이터셋
- uspto-grants-2016_08
- 특허 번호
- US09409905B2
반응 노트
불러오는 중…