Hydrochloric Acid → HCID 67520382, compound
Reaction equation
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([N:14]([C:18]2[CH:22]=[CH:21][S:20][C:19]=2[C:23]([O:25][CH3:26])=[O:24])COC)(=[O:13])=[O:12])=[C:7]([CH:27]=[CH:28][C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[CH:6]=1)([CH3:4])([CH3:3])[CH3:2].Cl>O1CCCC1>[C:1]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([NH:14][C:18]2[CH:22]=[CH:21][S:20][C:19]=2[C:23]([O:25][CH3:26])=[O:24])(=[O:13])=[O:12])=[C:7]([CH:27]=[CH:28][C:29]2[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=2)[CH:6]=1)([CH3:4])([CH3:2])[CH3:3]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 75 °C
Procedure
To a solution of 25 (134.0 mg; 0.27 mmol) in tetrahydrofuran (8 mL) was added aqueous hydrochloric acid (8.0 mL; 16.0 mmol; 2N). The reaction mixture was heated at 75° C. for 4 hours, and then additional aqueous hydrochloric acid (3.0 mL; 6N) was added and the reaction mixture further heated at reflux for 4-5 hours. The reaction mixture was allowed to cool to room temperature and then extracted with ethyl acetate (15 mL). The organic layer was separated, dried over magnesium sulfate, filtered and concentrated under reduced pressure to yield an orange oil residue which was purified by automated silica gel chromatography (Biotage®) eluting with ethyl acetate/hexanes (0 to 30% v/v over 400 mL gradient elution) to yield the title product as a white solid (60.9 mg).
Workup
- temperaturethe reaction mixture further heated
- temperatureat reflux for 4-5 hours
- temperatureto cool to room temperature
- extractionextracted with ethyl acetate (15 mL)
- customThe organic layer was separated
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customto yield an orange oil residue which
- customwas purified by automated silica gel chromatography (Biotage®)
- washeluting with ethyl acetate/hexanes (0 to 30% v/v over 400 mL gradient elution)
Sources & evidence
- ORD record
- ord-cd019ab2c02842ecb2c76493af6fe7ae
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08178699B2
Reaction notes
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