반응식
[OH:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=O.C([NH:29][CH2:30][CH2:31][N:32]1[C:36](=[O:37])[CH2:35][S:34][C:33]1=[O:38])(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.N1CCCCC1.NCCN1C(=O)/C(=C/C2C=CC=CC=2)/SC1=O>>[NH2:29][CH2:30][CH2:31][N:32]1[C:36](=[O:37])/[C:35](=[CH:4]/[C:3]2[CH:6]=[CH:7][CH:8]=[CH:9][C:2]=2[OH:1])/[S:34][C:33]1=[O:38]참가 물질
5
실험 절차
The title compound 30i was prepared from 2-hydroxybenzaldehyde (76 mg, 0.62 mmol), compound 29 (250 mg, 0.62 mmol) and piperidine (20.0 μL, 0.19 mmol) in a manner similar to that described for 30a in 50.0% (117 mg) yield as a yellow solid.
후처리
- customyield as a yellow solid
출처 및 근거
- ORD 기록
- ord-b62b2550bf8d4680b5bdab13d3cac635
- 출처 데이터셋
- uspto-grants-2015_08
- 특허 번호
- US09115122B2
연결된 노트
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