1,1'-Carbonyldiimidazole → HCID 69970027, compound
Reaction equation
[NH2:1][CH2:2][CH2:3][NH:4][CH:5]1[CH2:10][CH2:9][N:8]([CH2:11][CH2:12][C@@H:13]([C:25]2[CH:30]=[CH:29][C:28]([Cl:31])=[C:27]([Cl:32])[CH:26]=2)[CH2:14][N:15]([CH3:24])[C:16](=[O:23])[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH2:7][CH2:6]1.[C:33](N1C=CN=C1)(N1C=CN=C1)=[O:34]>C(Cl)(Cl)Cl.ClCCl>[ClH:31].[Cl:32][C:27]1[CH:26]=[C:25]([C@H:13]([CH2:12][CH2:11][N:8]2[CH2:9][CH2:10][CH:5]([N:4]3[CH2:3][CH2:2][NH:1][C:33]3=[O:34])[CH2:6][CH2:7]2)[CH2:14][N:15]([CH3:24])[C:16](=[O:23])[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH:30]=[CH:29][C:28]=1[Cl:31]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A stirred solution of (S)-N-[4-[4-(2-aminoethylamino)-piperidino]-2-(3,4-dichlorophenyl)butyl]-N-methylbenzamide (0.356 g) and 1,1'-carbonyldiimidazole (0.157 g) in chloroform (6 mL) was heated at reflux for 2 hours. The reaction mixture was diluted with dichloromethane, washed (aqueous sodium bicarbonate), dried, evaporated, and chromatographed, with dichloromethane:methanol (gradient 98:2, 90:10) as eluent. The resulting material was dissolved in dichloromethane, precipitated as the hydrochloride salt with ethereal hydrogen chloride, evaporated, and placed under high vacuum overnight to give the title compound as a white solid (0.244 g); MS: m/z=503(M+1); Analysis for C26H32Cl2N4O2.1.70 HCl.0.20 (C2H5)2O: Calculated: C, 55.47; H, 6.20; N, 9.65; Found: C, 55.47; H, 6.35; N, 9.44.
Workup
- temperatureat reflux for 2 hours
- washwashed (aqueous sodium bicarbonate)
- customdried
- customevaporated
- customchromatographed, with dichloromethane
- dissolutionThe resulting material was dissolved in dichloromethane
- customprecipitated as the hydrochloride salt with ethereal hydrogen chloride
- customevaporated
- customplaced under high vacuum overnight
Sources & evidence
- ORD record
- ord-e48691f97b814faf9e78ef1124d9d20c
- Source dataset
- uspto-grants-1999_11
- Patent number
- US05990130
Reaction notes
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