Isopropanol → HCID 178484077, compound
Reaction equation
C([O:5][C:6]([CH2:8][O:9][C:10]1[CH:11]=[CH:12][C:13]2[O:17][C:16]([C:18]([NH:20][C:21]3[CH:26]=[CH:25][C:24]([Cl:27])=[CH:23][N:22]=3)=[O:19])=[C:15]([NH:28][C:29]([C@H:31]3[CH2:36][CH2:35][C@H:34]([N:37]([CH3:39])[CH3:38])[CH2:33][CH2:32]3)=[O:30])[C:14]=2[CH:40]=1)=[O:7])(C)(C)C.C(O)(C)C>Cl>[ClH:27].[C:6]([CH2:8][O:9][C:10]1[CH:11]=[CH:12][C:13]2[O:17][C:16]([C:18]([NH:20][C:21]3[CH:26]=[CH:25][C:24]([Cl:27])=[CH:23][N:22]=3)=[O:19])=[C:15]([NH:28][C:29]([C@H:31]3[CH2:36][CH2:35][C@H:34]([N:37]([CH3:38])[CH3:39])[CH2:33][CH2:32]3)=[O:30])[C:14]=2[CH:40]=1)([OH:7])=[O:5]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Trans-5-t-butoxycarbonylmethoxy-3-[4-(dimethylamino)-cyclohexylcarbonylamino]-N-(5-chloropyridin-2-yl)benzofuran-2-carboxamide (1.92 g) obtained in Example 31 is dissolved in 6N hydrochloric acid (40 ml), and the mixture is stirred at room temperature for 2 hours. To the reaction solution is added isopropanol (100 ml), and the precipitated solid is collected by filtration, washed with isopropanol and diethyl ether, and dried under reduced pressure to give the title compound (1.86 g).
Workup
- filtrationthe precipitated solid is collected by filtration
- washwashed with isopropanol and diethyl ether
- customdried under reduced pressure
Sources & evidence
- ORD record
- ord-3901d0f3171e4c4da45d5032046004f5
- Source dataset
- uspto-grants-2009_05
- Patent number
- US07531537B2
Reaction notes
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