Trifluoroacetic acid → HCID 117697841, compound
Reaction equation
[CH2:1]([O:3][C:4](=[O:23])[CH2:5][CH:6]1[CH2:13][CH:12]2[N:14](C(OC(C)(C)C)=O)[CH:8]([CH2:9][O:10][CH2:11]2)[CH:7]1[OH:22])[CH3:2].FC(F)(F)C(O)=O>ClCCl>[OH:22][CH:7]1[CH:6]([CH2:5][C:4]([O:3][CH2:1][CH3:2])=[O:23])[CH2:13][CH:12]2[NH:14][CH:8]1[CH2:9][O:10][CH2:11]2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of compound 123d (100 mg) in dichloromethane (2.0 mL) was added trifluoroacetic acid (1.0 mL). The reaction mixture was stirred at room temperature for one hour, and concentrated under reduced pressure to give ethyl 2-(6-hydroxy-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)acetate 123a, which was used directly in next step without purification.
Workup
- concentrationconcentrated under reduced pressure
Sources & evidence
- ORD record
- ord-75d670500ab64065ae6c5c78d4f18a63
- Source dataset
- uspto-grants-2016_02
- Patent number
- US09266904B2
Reaction notes
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