Hydrochloric Acid → HCID 53357876, compound
Reaction equation
[Cl:1][C:2]1[C:3]([F:44])=[C:4]([C@@H:8]2[C@:12]([C:15]3[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][C:16]=3[F:22])([C:13]#[N:14])[C@H:11]([CH2:23][C:24]([CH3:27])([CH3:26])[CH3:25])[NH:10][C@H:9]2[C:28]([NH:30][C:31]2[CH:36]=[CH:35][C:34]([CH2:37][CH2:38][CH2:39][C:40]([O:42]C)=[O:41])=[CH:33][CH:32]=2)=[O:29])[CH:5]=[CH:6][CH:7]=1.O.[OH-].[Li+].Cl>C1COCC1.O>[Cl:1][C:2]1[C:3]([F:44])=[C:4]([C@@H:8]2[C@:12]([C:15]3[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][C:16]=3[F:22])([C:13]#[N:14])[C@H:11]([CH2:23][C:24]([CH3:27])([CH3:26])[CH3:25])[NH:10][C@H:9]2[C:28]([NH:30][C:31]2[CH:32]=[CH:33][C:34]([CH2:37][CH2:38][CH2:39][C:40]([OH:42])=[O:41])=[CH:35][CH:36]=2)=[O:29])[CH:5]=[CH:6][CH:7]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of chiral methyl 4-(4-((2R,3S,4R,5S)-3-(3-chloro-2-fluorophenyl)-4-(4-chloro-2-fluorophenyl)-4-cyano-5-neopentylpyrrolidine-2-carboxamido)phenyl)butanoate (70.5 mg, 0.110 mmol) in THF (5 ml) was treated with LITHIUM HYDROXIDE MONOHYDRATE (18.5 mg, 0.441 mmol) in water (2.5 ml) and stirred at rt for 16 hrs. The reaction was treated with 1 N HCl (pH 5) and extracted with ethyl acetate, washed with water then sat'd sodium chloride, dried with sodium sulfate, filtered and lyophilized to give chiral-4-(4-((2R,3S,4R,5S)-3-(3-chloro-2-fluorophenyl)-4-(4-chloro-2-fluorophenyl)-4-cyano-5-neopentylpyrrolidine-2-carboxamido)phenyl)butanoic acid (67 mg, 97.2%) as a white lyophilized solid. MS (ES+) m/z Calcd: [(M+H)+]: 628.19. found: 628.1.
Workup
- extractionextracted with ethyl acetate
- washwashed with water
- dry with materialdried with sodium sulfate
- filtrationfiltered
Sources & evidence
- ORD record
- ord-071136eeb87f4b8099234f5033799f5c
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08354444B2
Reaction notes
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