Hydrochloric Acid → HCID 16224812, compound

HRID 390646Notes

Reaction equation

[OH-].[Na+].[CH2:3]([O:7][C:8]1[CH:13]=[C:12](/[CH:14]=[C:15](\[O:20][CH3:21])/[C:16]([O:18]C)=[O:17])[CH:11]=[CH:10][C:9]=1[C:22]1[CH:27]=[CH:26][CH:25]=[C:24]([N:28]([CH3:36])[C:29]([NH:31][CH2:32][CH2:33][CH2:34][CH3:35])=[O:30])[CH:23]=1)[CH2:4][CH2:5][CH3:6].Cl.O>O1CCCC1.C(OCC)(=O)C>[CH2:3]([O:7][C:8]1[CH:13]=[C:12](/[CH:14]=[C:15](\[O:20][CH3:21])/[C:16]([OH:18])=[O:17])[CH:11]=[CH:10][C:9]=1[C:22]1[CH:27]=[CH:26][CH:25]=[C:24]([N:28]([CH3:36])[C:29]([NH:31][CH2:32][CH2:33][CH2:34][CH3:35])=[O:30])[CH:23]=1)[CH2:4][CH2:5][CH3:6]

Participants

Conditions

Temperature: 68 °C

Procedure

0.65 mL (0.65 mmol) of aqueous 1 M sodium hydroxide solution is added to a solution of 0.2 g (0.43 mmol) of methyl (Z)-3-[2-butoxy-3′-(1-methyl-3-butylureido)biphenyl-4-yl]-2-methoxyacrylate in 5 mL of tetrahydrofuran. The reaction mixture is stirred at 68° C. for 5 hours. After cooling, the reaction is stopped by addition of 1 mL aqueous 1 M hydrochloric acid solution and 10 mL of water and extraction with ethyl acetate. The organic phases are combined, washed with saturated sodium chloride solution and then dried over magnesium sulfate. The solvents are evaporated off. The product is recrystallized from a pentane/acetone mixture to give 0.12 g (63%) of (Z)-3-[2-butoxy-3′-(1-methyl-3-butylureido)biphenyl-4-yl]-2-methoxyacrylic acid in the form of a white solid with a melting point of 106° C.

Workup

temperatureAfter cooling
washwashed with saturated sodium chloride solution
dry with materialdried over magnesium sulfate
customThe solvents are evaporated off
customThe product is recrystallized from a pentane/acetone mixture

Sources & evidence

ORD record: ord-8a03522bc13b4084b65491a6d8eaa276
Source dataset: uspto-grants-2013_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08383652B2

Reaction notes

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