Hydrochloric Acid → HCID 178484810, compound
Reaction equation
C(O[C:6]([N:8]([C@H:10]1[CH2:15][CH2:14][C@H:13]([C:16]([NH:18][C:19]2[C:23]3[CH:24]=[C:25]([C:28]([O:30][CH3:31])=[O:29])[CH:26]=[CH:27][C:22]=3[O:21][C:20]=2[C:32]([NH:34][C:35]2[CH:40]=[CH:39][C:38]([Cl:41])=[CH:37][N:36]=2)=[O:33])=[O:17])[CH2:12][CH2:11]1)C)=O)(C)(C)C.Cl>O1CCOCC1.C(OCC)C>[ClH:41].[CH3:31][O:30][C:28]([C:25]1[CH:26]=[CH:27][C:22]2[O:21][C:20]([C:32]([NH:34][C:35]3[CH:40]=[CH:39][C:38]([Cl:41])=[CH:37][N:36]=3)=[O:33])=[C:19]([NH:18][C:16]([C@H:13]3[CH2:12][CH2:11][C@H:10]([NH:8][CH3:6])[CH2:15][CH2:14]3)=[O:17])[C:23]=2[CH:24]=1)=[O:29]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Trans-3-[4-(N-t-butoxycarbonyl-N-methylamino)cyclohexylcarbonylamino]-5-methoxycarbonyl-N-(5-chloropyridin-2-yl)benzofuran-2-carboxamide (4.60 g) obtained in Example 202 is dissolved in dioxane (20 ml), and thereto is added 4N hydrogen chloride in dioxane (10 ml), and the mixture is stirred at room temperature for 48 hours. The reaction solution is diluted with diethyl ether, and the precipitates are collected by filtration, washed several times with diethyl ether and dried to give the title compound (4.02 g).
Workup
- filtrationthe precipitates are collected by filtration
- washwashed several times with diethyl ether
- customdried
Sources & evidence
- ORD record
- ord-f7a6f507f8e642b993af44d4e7821d9e
- Source dataset
- uspto-grants-2009_05
- Patent number
- US07531537B2
Reaction notes
Loading…