Ethanol → HCID 24985023, 화합물
반응식
[C:1]1([C@H:7]([NH:9][C:10]2[C:15]([N+:16]([O-])=O)=CN=[C:12]([C:19]3[CH:28]=[CH:27][CH:26]=[C:25]4[C:20]=3[CH:21]=[CH:22][CH:23]=[N:24]4)[CH:11]=2)[CH3:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C1([C@H](NC2C=C(C3C=CC=C4C=3C=CC=N4)N=C[C:39]=2[NH2:54])C)C=CC=CC=1.[H][H].[CH2:57]([OH:59])C>[Pd]>[C:1]1([C@H:7]([N:9]2[C:10]3[C:15](=[N:54][CH:39]=[C:12]([C:19]4[CH:28]=[CH:27][CH:26]=[C:25]5[C:20]=4[CH:21]=[CH:22][CH:23]=[N:24]5)[CH:11]=3)[NH:16][C:57]2=[O:59])[CH3:8])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1참가 물질
5
실험 절차
((1R)-1-phenylethyl)(3-amino-6-(5-quinolyl)(4-pyridyl))amine ((1R)-1-Phenylethyl)(5-nitro-2-(5-quinolyl)(4-pyridyl))amine (500 mg, 1.35 mmol) was dissolved in ethanol (100 mL). Palladium on carbon (70 mg) was added followed by a hydrogen balloon. The reaction was stirred at room temperature for 18 h, then filtered through celite. The filtrate was condensed under reduced pressure to afford the desired product (450 mg, 97.9%). (MS (ESI) m/z 341 [M+1]+.
후처리
- filtrationfiltered through celite
- customcondensed under reduced pressure
출처 및 근거
- ORD 기록
- ord-ebef9d952b684c2ca9414dd62f5fef6f
- 출처 데이터셋
- uspto-grants-2013_02
- 특허 번호
- US08372976B2
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