Sodium Hydroxide → 2-butyl-3-[5-(1-carboxycyclopent-3-enyl)thiophen-2-ylmethyl]-5-chloro-3H-imidazole-4-carboxylic acid
反応式
C([O:3][C:4]([C:6]1[N:7]([CH2:16][C:17]2[S:18][C:19]([C:22]3([C:27]([O:29]CC)=[O:28])[CH2:26][CH:25]=[CH:24][CH2:23]3)=[CH:20][CH:21]=2)[C:8]([CH2:12][CH2:13][CH2:14][CH3:15])=[N:9][C:10]=1[Cl:11])=[O:5])C.[OH-].[Na+]>CO>[CH2:12]([C:8]1[N:7]([CH2:16][C:17]2[S:18][C:19]([C:22]3([C:27]([OH:29])=[O:28])[CH2:26][CH:25]=[CH:24][CH2:23]3)=[CH:20][CH:21]=2)[C:6]([C:4]([OH:5])=[O:3])=[C:10]([Cl:11])[N:9]=1)[CH2:13][CH2:14][CH3:15]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of the product of Step 1, above (71) (50 mg) in 2 ml of methanol was added 1 ml 2N NaOH. This mixture was stirred at ambient temperature for 2 hours, the solvent was removed and the residue taken up in water and extracted (2×EtOAc). The aqueous layer was then acidified with 10% HCl and extracted (3×EtOAc). The combined organics were dried over MgSO4, filtered and concentrated to dryness to yield the title compound (72).