Chlorine → HCID 178462058, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[C:11]([N:13]1[CH2:17][CH:16]=[CH:15][CH2:14]1)=[O:12])[C:5]([OH:7])=O.CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.C(N(C(C)C)CC)(C)C.[Cl:49][C:50]1[CH:61]=[CH:60][C:53]2[NH:54][C:55]([C@@H:57]([NH2:59])[CH3:58])=[N:56][C:52]=2[CH:51]=1.ClCl>O1CCCC1.ClCCl.C(O)C>[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[C:11]([N:13]1[CH2:17][CH:16]=[CH:15][CH2:14]1)=[O:12])[C:5]([NH:59][C@H:57]([C:55]1[NH:54][C:53]2[CH:60]=[CH:61][C:50]([Cl:49])=[CH:51][C:52]=2[N:56]=1)[CH3:58])=[O:7]Participants
8
Reactant 5
Product 1
Reagents, catalysts & solvents 2
Procedure
Prepared analogously to Example 1 g from 3-chloro-4-(2,5-dihydropyrrol-1-ylcarbonyl)benzoic acid, TBTU, diisopropylethylamine, and (1S)-1-(5-chloro-1H-benzimidazol-2-yl)ethylamine in tetrahydrofuran. Yield: quantitative; Rf value: 0.50 (silica gel: dichloromethane/ethanol=9:1); C21H18Cl2N4O2 (429.305); mass spectrum: (M+H)+=429/431/433 (chlorine isotope).
Sources & evidence
- ORD record
- ord-b6bbd19e6ccd4f2b9fede6532e8540a0
- Source dataset
- uspto-grants-2008_02
- Patent number
- US07326791B2
Reaction notes
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