Hydrochloric Acid → HCID 53357876, compound

HRID 1807292Notes

Reaction equation

HRID 1807292 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]=1

Participants

6

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

  1. extractionextracted with ethyl acetate
  2. washwashed with water
  3. dry with materialdried with sodium sulfate
  4. filtrationfiltered

Sources & evidence

ORD record
ord-071136eeb87f4b8099234f5033799f5c
Source dataset
uspto-grants-2013_01
Patent number
US08354444B2

Reaction notes

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