Hydrochloric Acid → (R)-3-{4-[3-(3-Bromophenyl)-1-(4-cyclohexylphenyl)ureidomethyl]benzoylamino}-2-hydroxypropionic acid

HRID 412436Notes

Reaction equation

HRID 412436 reaction equation
C([O:3][C:4](=[O:41])[C@H:5]([OH:40])[CH2:6][NH:7][C:8](=[O:39])[C:9]1[CH:14]=[CH:13][C:12]([CH2:15][N:16]([C:27]2[CH:32]=[CH:31][C:30]([CH:33]3[CH2:38][CH2:37][CH2:36][CH2:35][CH2:34]3)=[CH:29][CH:28]=2)[C:17]([NH:19][C:20]2[CH:25]=[CH:24][CH:23]=[C:22]([Br:26])[CH:21]=2)=[O:18])=[CH:11][CH:10]=1)C.[OH-].[Na+].Cl>C(O)C>[Br:26][C:22]1[CH:21]=[C:20]([NH:19][C:17](=[O:18])[N:16]([CH2:15][C:12]2[CH:11]=[CH:10][C:9]([C:8]([NH:7][CH2:6][C@@H:5]([OH:40])[C:4]([OH:41])=[O:3])=[O:39])=[CH:14][CH:13]=2)[C:27]2[CH:32]=[CH:31][C:30]([CH:33]3[CH2:34][CH2:35][CH2:36][CH2:37][CH2:38]3)=[CH:29][CH:28]=2)[CH:25]=[CH:24][CH:23]=1

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 67483100(R)-3-{4-[3-(3-bromophenyl)-1-(4-cyclohexylphenyl)ureidomethyl]benzoylamino}-2-hydroxypropionic acid ethyl ester

Product 1

HCID 10282059(R)-3-{4-[3-(3-Bromophenyl)-1-(4-cyclohexylphenyl)ureidomethyl]benzoylamino}-2-hydroxypropionic acidYield 39.8%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

(R)-3-{4-[3-(3-Bromophenyl)-1-(4-cyclohexylphenyl)ureidomethyl]benzoylamino}-2-hydroxypropionic acid ethyl ester (100 mg) was dissolved in ethanol (10 mL), 1 N sodium hydroxide (480 μL) was added and the resulting mixture was stirred at room temperature for 1 hour. 1 N Hydrochloric acid (480 μL) was added and the mixture was concentrated in vacuo. The residue was suspended in water (50 mL) and filtered to afford 38 mg of the title compound.

Workup

  1. concentrationthe mixture was concentrated in vacuo
  2. filtrationfiltered

Sources & evidence

ORD record
ord-7f8a3ab8fdb049d9abbebf0ce6e603e8
Source dataset
uspto-grants-2003_05
Patent number
US06562807B2

Reaction notes

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