Hydrochloric Acid → HCID 86712976, compound
Reaction equation
[Si]([O:8][CH2:9][C:10]1([CH3:34])[S:16][CH2:15][CH2:14][N:13]2[C:17]([C:20]3([C:23]4[CH:28]=[CH:27][C:26]([C:29]5[O:30][CH:31]=[CH:32][N:33]=5)=[CH:25][CH:24]=4)[CH2:22][CH2:21]3)=[N:18][N:19]=[C:12]2[CH2:11]1)(C(C)(C)C)(C)C.Cl>CO>[CH3:34][C:10]1([CH2:9][OH:8])[S:16][CH2:15][CH2:14][N:13]2[C:17]([C:20]3([C:23]4[CH:24]=[CH:25][C:26]([C:29]5[O:30][CH:31]=[CH:32][N:33]=5)=[CH:27][CH:28]=4)[CH2:22][CH2:21]3)=[N:18][N:19]=[C:12]2[CH2:11]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of the compound (260 mg, 0.52 mmol) obtained in Example 84-1) and 4 M hydrochloric acid (1,4-dioxane solution, 3 mL) in methanol (6 mL) was stirred overnight at room temperature. The reaction mixture was concentrated under reduced pressure, a 5 M aqueous sodium hydroxide solution (10 mL) was added to the residue, the mixture was extracted with ethyl acetate, and the organic layer was washed with saturated sodium chloride solution and dried with anhydrous sodium sulfate. After concentration under reduced pressure, the residue was purified by silica gel chromatography (ethyl acetate:methanol=20:80) to obtain the title compound (172 mg, 87%) as a colorless solid.
Workup
- concentrationThe reaction mixture was concentrated under reduced pressure
- additiona 5 M aqueous sodium hydroxide solution (10 mL) was added to the residue
- extractionthe mixture was extracted with ethyl acetate
- washthe organic layer was washed with saturated sodium chloride solution
- dry with materialdried with anhydrous sodium sulfate
- concentrationAfter concentration under reduced pressure
- customthe residue was purified by silica gel chromatography (ethyl acetate:methanol=20:80)
Sources & evidence
- ORD record
- ord-c9c8de1f8d52467ca15452727c3f9d3b
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08927536B2
Reaction notes
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