Ethanol → HCID 23109914, compound
Reaction equation
[ClH:1].C(OCC)(=O)C.[N:8]1[CH:13]=[CH:12][C:11]([CH2:14][N:15]([CH2:47][C:48]2[CH:53]=[CH:52][N:51]=[CH:50][CH:49]=2)[CH2:16][CH2:17][C:18]2([CH2:24][CH2:25][N:26]3[CH2:31][CH2:30][CH:29]([N:32]([C:40]4[CH:45]=[CH:44][C:43]([CH3:46])=[CH:42][CH:41]=4)[C:33]([C:35]4[O:36][CH:37]=[CH:38][CH:39]=4)=[O:34])[CH2:28][CH2:27]3)[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]2)=[CH:10][CH:9]=1.C(O)C>C(OCC)(=O)C>[ClH:1].[ClH:1].[ClH:1].[ClH:1].[N:51]1[CH:52]=[CH:53][C:48]([CH2:47][N:15]([CH2:14][C:11]2[CH:10]=[CH:9][N:8]=[CH:13][CH:12]=2)[CH2:16][CH2:17][C:18]2([CH2:24][CH2:25][N:26]3[CH2:31][CH2:30][CH:29]([N:32]([C:40]4[CH:41]=[CH:42][C:43]([CH3:46])=[CH:44][CH:45]=4)[C:33]([C:35]4[O:36][CH:37]=[CH:38][CH:39]=4)=[O:34])[CH2:28][CH2:27]3)[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]2)=[CH:49][CH:50]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
After adding a 4N hydrochloric acid/ethyl acetate solution (0.35 mL, 1.4 mmol) to a solution of N-[1-[2-[1-[2-[bis(pyridin-4-ylmethyl)amino]ethyl]cyclohexyl]ethyl]piperidin-4-yl]-N-(p-tolyl)-2-furancarboxamide (171 mg, 0.28 mmol) in ethyl acetate (2 mL)-ethanol (2 mL), the mixture was stirred at room temperature for 10 minutes. Ethyl acetate (3 mL) was added to the reaction mixture, and after stirring for 20 minutes in an ice bath, the precipitated crystals were filtered out and dried under reduced pressure to obtain the title compound as a white solid (136 mg, 0.18 mmol) (64% yield).
Workup
- stirringafter stirring for 20 minutes in an ice bath
- filtrationthe precipitated crystals were filtered out
- customdried under reduced pressure
Sources & evidence
- ORD record
- ord-3f77e5b0528a4d36b40e86f525cf5b78
- Source dataset
- uspto-grants-2009_10
- Patent number
- US07601843B2
Reaction notes
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