Hydrochloric Acid → HCID 117759805, compound

HRID 1049437Notes

Reaction equation

[CH:1]1([CH:4]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([CH2:17][S:18]([C:21]3[CH:26]=[CH:25][C:24]([C:27]4[CH:32]=[C:31]([O:33][CH3:34])[CH:30]=[CH:29][C:28]=4[F:35])=[C:23]([CH2:36][C:37]([CH3:40])([CH3:39])[CH3:38])[CH:22]=3)(=[O:20])=[O:19])[CH:12]=2)[CH2:5][C:6]([O:8]CC)=[O:7])[CH2:3][CH2:2]1.[OH-].[Na+].Cl>C(O)C>[CH:1]1([CH:4]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([CH2:17][S:18]([C:21]3[CH:26]=[CH:25][C:24]([C:27]4[CH:32]=[C:31]([O:33][CH3:34])[CH:30]=[CH:29][C:28]=4[F:35])=[C:23]([CH2:36][C:37]([CH3:40])([CH3:39])[CH3:38])[CH:22]=3)(=[O:20])=[O:19])[CH:12]=2)[CH2:5][C:6]([OH:8])=[O:7])[CH2:2][CH2:3]1

Participants

Conditions

Temperature: 50 °C

Procedure

To a solution of ethyl 3-cyclopropyl-3-(3-(((2′-fluoro-5′-methoxy-2-neopentyl-[1,1′-biphenyl]-4-yl)sulfonyl)methyl)phenyl)propanoate (204 mg) in ethanol (3.6 mL) was added 2N aqueous sodium hydroxide solution (898 μl) at room temperature, and the mixture was stirred at 50° C. for 2 hr. The reaction mixture was cooled to 0° C., neutralized with 1N hydrochloric acid, and extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give the title compound (133 mg) as a white amorphous solid.

Workup

temperatureThe reaction mixture was cooled to 0° C.
extractionextracted with ethyl acetate
washThe extract was washed with saturated brine
dry with materialdried over anhydrous sodium sulfate
customThe solvent was evaporated under reduced pressure

Sources & evidence

ORD record: ord-e05032ff0a1d402aa85b3bd2a60619a5
Source dataset: uspto-grants-2016_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09382188B2

Reaction notes

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