Hydrochloric Acid → 1-[6-(4-{(S)-1-[(S)-6-(2-hydroxy-2-methyl-propyl)-2-oxo-6-phenyl-[1,3]oxazinan-3-yl]ethyl}-phenyl)-pyridazin-3-yl]-cyclopropanecarboxylic acid
Reaction equation
[OH-].[Na+].C([O:5][C:6]([C:8]1([C:11]2[N:12]=[N:13][C:14]([C:17]3[CH:22]=[CH:21][C:20]([CH:23]([N:25]4[CH2:30][CH2:29][C:28]([CH2:37][C:38]([OH:41])([CH3:40])[CH3:39])([C:31]5[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=5)[O:27][C:26]4=[O:42])[CH3:24])=[CH:19][CH:18]=3)=[CH:15][CH:16]=2)[CH2:10][CH2:9]1)=[O:7])C.Cl>CO>[OH:41][C:38]([CH3:39])([CH3:40])[CH2:37][C@@:28]1([C:31]2[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=2)[O:27][C:26](=[O:42])[N:25]([C@H:23]([C:20]2[CH:19]=[CH:18][C:17]([C:14]3[N:13]=[N:12][C:11]([C:8]4([C:6]([OH:7])=[O:5])[CH2:10][CH2:9]4)=[CH:16][CH:15]=3)=[CH:22][CH:21]=2)[CH3:24])[CH2:30][CH2:29]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
4 M aqueous NaOH solution (1.5 mL) was added to a solution of 1-[6-(4-{1-[6-(2-hydroxy-2-methylpropyl)-2-oxo-6-phenyl-[1,3]oxazinan-3-yl]-ethyl}-phenyl)-pyridazin-3-yl]-cyclopropane-carboxylic acid ethyl ester (0.81 g) in methanol (5 mL) at room temperature. The solution was stirred at room temperature for 2 h and was then neutralized with 1 M aqueous hydrochloric acid. Most of the methanol was evaporated, the residue was diluted with water, and the resulting mixture was extracted with ethyl acetate. The combined extracts were washed with brine, dried (Na2SO4), and concentrated to give the title compound as a solid. Yield: 0.72 g (93% of theory); LC (method 1): tR=1.44 min; Mass spectrum (ESI+): m/z=516 [M+H]+.
Workup
- customMost of the methanol was evaporated
- additionthe residue was diluted with water
- extractionthe resulting mixture was extracted with ethyl acetate
- washThe combined extracts were washed with brine
- dry with materialdried (Na2SO4)
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-8344ab4075c641f3a42c4f7ceeb360b5
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08933072B2
Reaction notes
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