HCID 43385182, compound → HCID 17956525, compound
Reaction equation
C([O:3][C:4](=[O:21])[CH2:5][NH:6][C:7]([NH:9][C:10]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[N:13]=[C:12](C)[CH:11]=1)=[O:8])C>Cl>[N:13]1[C:14]2[C:19](=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:10]([NH:9][C:7](=[O:8])[NH:6][CH2:5][C:4]([OH:21])=[O:3])=[CH:11][CH:12]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 80 °C
Procedure
[3-(2-Methyl-quinolin-4-yl)-ureido]-acetic acid ethyl ester (7.2 g, 25 mmol) is suspended in 6N aqueous HCl (250 mL), and the mixture is heated at 80° C. for 15 h. The mixture is cooled, filtered from the resulting precipitate and the solid dried to provide the title compound as hydrochloride salt.
Workup
- temperatureThe mixture is cooled
- filtrationfiltered from the resulting precipitate
- customthe solid dried
Sources & evidence
- ORD record
- ord-ff157d15e531489486eb617f453b1648
- Source dataset
- uspto-grants-2008_05
- Patent number
- US07375227B2
Reaction notes
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