Sodium Methoxide → HCID 86345769, 화합물
반응식
[O:1]1[CH2:6][CH2:5][N:4]([C:7]2[C:8]3[N:9]([CH:13]=[C:14](/[CH:16]=[CH:17]/[C:18]4[CH:27]=[C:26]([C:28]([OH:30])=[O:29])[C:25]5[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=5)[N:19]=4)[N:15]=3)[CH:10]=[CH:11][N:12]=2)[CH2:3][CH2:2]1.C[O-].[Na+:33]>CO>[Na+:33].[O:1]1[CH2:6][CH2:5][N:4]([C:7]2[C:8]3[N:9]([CH:13]=[C:14](/[CH:16]=[CH:17]/[C:18]4[CH:27]=[C:26]([C:28]([O-:30])=[O:29])[C:25]5[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=5)[N:19]=4)[N:15]=3)[CH:10]=[CH:11][N:12]=2)[CH2:3][CH2:2]1참가 물질
4
실험 절차
To a slurry of (E)-2-(2-(8-morpholinoimidazo[1,2-a]pyrazin-2-yl)vinyl)quinoline-4-carboxylic acid (32 mg, 0.08 mmol) in MeOH (0.6 mL), 1.5 M NaOMe in MeOH (0.16 mL, 0.08 mmol) was added. The resulting mixture was stirred for 10 min, concentrated, and dried under reduced pressure to obtain the title compound 8. 1H NMR (400 MHz, CD3OD) δ (ppm): 8.36 (d, J=8.6 Hz, 1H), 7.92-8.04 (m, 3H), 7.67-7.82 (m, 4H), 7.55 (t, J=7.6 Hz, 1H), 7.32 (d, J=4.4 Hz, 1H), 4.24-4.32 (m, 4H), 3.89 (t, 4H). Mass Spectrum (LCMS, ESI pos.) Calcd. For C22H19N5O3: 402.2 (M+H). Found 402.4.
후처리
- concentrationconcentrated
- customdried under reduced pressure
출처 및 근거
- ORD 기록
- ord-877d75f1e3ee4477887d05926b818631
- 출처 데이터셋
- uspto-grants-2016_02
- 특허 번호
- US09249163B2
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