HCID 59631474, compound → HCID 59631171, compound
Reaction equation
[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:18])=[C:6]([NH:8][C:9](=[O:17])[CH:10]([CH3:16])[C:11]([O:13]CC)=[O:12])[CH:7]=1>C1COCC1>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:18])=[C:6]([NH:8][C:9](=[O:17])[CH:10]([CH3:16])[C:11]([OH:13])=[O:12])[CH:7]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The acid was prepared according to procedure B using ethyl 3-(5-fluoro-2-methylphenylamino)-2-methyl-3-oxopropanoate (2.45 g, 9.67 mmol) in THF (9.67 mL). The crude product was used without further purification. Mass Spectrum (ESI) m/e=226.0, (M+1).
Workup
- customThe acid was prepared
- customThe crude product was used without further purification
Sources & evidence
- ORD record
- ord-535f9563fdad4d80a27012b98fc4f585
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08765940B2
Reaction notes
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