Hydrochloric Acid → HCID 59026159, compound
Reaction equation
[OH:1][C@H:2]1[C@@H:6]([CH2:7][NH:8][C:9](=[O:14])[C:10]([F:13])([F:12])[F:11])[CH2:5][N:4](C(OC(C)(C)C)=O)[CH2:3]1.Cl.O1CCOCC1>C(Cl)Cl>[F:13][C:10]([F:11])([F:12])[C:9]([NH:8][CH2:7][C@@H:6]1[C@H:2]([OH:1])[CH2:3][NH:4][CH2:5]1)=[O:14]Participants
5
Procedure
(1,1-dimethylethyl(3S,4S)-3-hydroxy-4-{[(trifluoroacetyl)amino]methyl}-1-pyrrolidinecarboxylate (0.192 g, 0.615 mmol) was dissolved in methylene chloride (5 mL). HCl in dioxane (1.0 mL, 4.0 mmol) was added and the solution stirred at ambient temperature for 2 hours. The solvent was removed under reduced pressure. (0.137 g, quant.) LCMS: m/z 213.2 (MH+).
Workup
- customThe solvent was removed under reduced pressure
Sources & evidence
- ORD record
- ord-1d94b506e4e54df5b517cd237cf2493c
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07691850B2
Reaction notes
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