Ammonia → 5-Acetyl-8-amino-1-(1,3-benzodioxol-5-yl)-4,5-dihydro-1h-pyrazolo[4,3-c]quinoline-3-carboxamide acetate
반응식
[C:1]([N:4]1[C:13]2[CH:12]=[CH:11][C:10]([NH2:14])=[CH:9][C:8]=2[C:7]2[N:15]([C:23]3[CH:31]=[CH:30][C:26]4[O:27][CH2:28][O:29][C:25]=4[CH:24]=3)[N:16]=[C:17]([C:18]([O:20]CC)=[O:19])[C:6]=2[CH2:5]1)(=[O:3])[CH3:2].[NH3:32]>C(O)C>[C:18]([OH:20])(=[O:19])[CH3:17].[C:1]([N:4]1[C:13]2[CH:12]=[CH:11][C:10]([NH2:14])=[CH:9][C:8]=2[C:7]2[N:15]([C:23]3[CH:31]=[CH:30][C:26]4[O:27][CH2:28][O:29][C:25]=4[CH:24]=3)[N:16]=[C:17]([C:18]([NH2:32])=[O:20])[C:6]=2[CH2:5]1)(=[O:3])[CH3:2]참가 물질
4
반응 조건
- 온도
- 120 °C
실험 절차
The material of Step 5 (450 mg, 0.00094 mol) was dissolved in ethanol (10 mL) and NH3 (10 mL), and the resulting reaction mixture was heated to 120° C. and shaken for 20 hours at 600 psi. The reaction was then cooled and vented for 2 hours. The resulting solution was concentrated in vacuo to give the product as a brown glass. 340 mg (MW=391.38, 93% yield). LC/MS m/z=392.05 (m+1).
후처리
- temperatureThe reaction was then cooled
- waitvented for 2 hours
- concentrationThe resulting solution was concentrated in vacuo
출처 및 근거
- ORD 기록
- ord-7aef8dee30e047c495af187b3b0aa7d9
- 출처 데이터셋
- uspto-grants-2007_05
- 특허 번호
- US07211597B2
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