p-Toluenesulfonic acid monohydrate → HCID 86614637, compound
Reaction equation
O.[C:2]1([CH3:12])[CH:7]=[CH:6][C:5]([S:8]([OH:11])(=[O:10])=[O:9])=[CH:4][CH:3]=1.[F:13][CH2:14][C@H:15]1[CH2:19][CH2:18][N:17](C(OC(C)(C)C)=O)[CH2:16]1>C(O)C>[CH3:12][C:2]1[CH:3]=[CH:4][C:5]([S:8]([OH:11])(=[O:10])=[O:9])=[CH:6][CH:7]=1.[F:13][CH2:14][C@H:15]1[CH2:19][CH2:18][NH:17][CH2:16]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Prepare using the method of Intermediate 49 with p-toluenesulfonic acid monohydrate (0.14 g, 0.74 mmol), tert-butyl (3S)-3-(fluoromethyl)pyrrolidine-1-carboxylate (See Intermediate 54) (0.15 g, 0.74 mmol) and ethanol (2 mL) to give the title compound as a white solid (0.20 g): MS (m/e): 104 (M+1).
Workup
- customPrepare
Sources & evidence
- ORD record
- ord-4e382542736f41c79a745babf70b4591
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07666871B2
Reaction notes
Loading…