Hydrochloric Acid → HCID 86615020, compound
Reaction equation
[ClH:1].C(OC([N:9]1[CH2:13][C@H:12]([O:14][C:15](=[O:21])[NH:16][C:17]([CH3:20])([CH3:19])[CH3:18])[CH2:11][C@@H:10]1[C@H:22]1[O:26]C(C)(C)[N:24]([C:29](=[O:31])[CH3:30])[C@H:23]1[CH2:32][C:33]1[CH:38]=[C:37]([F:39])[CH:36]=[C:35]([F:40])[CH:34]=1)=O)(C)(C)C>O1CCOCC1>[ClH:1].[C:29]([NH:24][C@@H:23]([CH2:32][C:33]1[CH:34]=[C:35]([F:40])[CH:36]=[C:37]([F:39])[CH:38]=1)[C@@H:22]([C@@H:10]1[NH:9][CH2:13][C@H:12]([O:14][C:15](=[O:21])[NH:16][C:17]([CH3:19])([CH3:18])[CH3:20])[CH2:11]1)[OH:26])(=[O:31])[CH3:30]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Add 4M hydrogen chloride in dioxane (5 mL) to (2R,4R)-2-[(4S,5S)-3-acetyl-4-(3,5-difluoro-benzyl)-2,2-dimethyl-oxazolidin-5-yl]-4-tert-butylcarbamoyloxy-pyrrolidine-1-carboxylic acid tert-butyl ester (0.34 g, 0.616 mmol). Stir 4 hours and evaporate to give the title compound as a foam (0.291 g, 100%).
Workup
- customevaporate
Sources & evidence
- ORD record
- ord-414b8a9aae1a448c89acb64bf8feaadc
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07585885B2
Reaction notes
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