Chlorine → HCID 178462059, 화합물
반응식
[Cl:1][C:2]1[CH:10]=[C:9]([C:11]([NH:13][C@H:14]([C:16]2[NH:20][C:19]3[CH:21]=[CH:22][C:23]([Cl:25])=[CH:24][C:18]=3[N:17]=2)[CH3:15])=[O:12])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.CN(C(ON1N=[N:41][C:36]2[CH:37]=[CH:38][CH:39]=[CH:40]C1=2)=[N+](C)C)C.[B-](F)(F)(F)F.[CH:48]([N:51](C(C)C)[CH2:52]C)(C)C.CN(CC1CCCN1)C.ClCl>O1CCCC1.CO>[Cl:1][C:2]1[CH:10]=[C:9]([CH:8]=[CH:7][C:3]=1[C:4]([N:41]1[CH2:36][CH2:37][CH2:38][C:39]1([CH3:40])[N:51]([CH3:52])[CH3:48])=[O:6])[C:11]([NH:13][C@H:14]([C:16]1[NH:20][C:19]2[CH:21]=[CH:22][C:23]([Cl:25])=[CH:24][C:18]=2[N:17]=1)[CH3:15])=[O:12]참가 물질
8
반응물 5
생성물 1
시약·촉매·용매 2
실험 절차
Prepared analogously to Example 1g from (1S)-2-chloro-4-{N-[1-(5-chloro-1H-benzimidazol-2-yl)ethyl]aminocarbonyl}benzoic acid, TBTU, diisopropylethylamine, and rac-2-(dimethylaminomethyl)pyrrolidine in tetrahydrofuran. Yield: 50%; Rf value: 0.32 (Reversed phase RP 8: methanol/5% sodium chloride solution=6:4); C24H27Cl2N5O2 (488.416); mass spectrum: (M+H)+=488/490/492 (chlorine isotope) and (M−H)−=486/488/490 (chlorine isotope).
출처 및 근거
- ORD 기록
- ord-131f705be09e48768738204722ea7ea7
- 출처 데이터셋
- uspto-grants-2008_02
- 특허 번호
- US07326791B2
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