Ethyl 2-methylacetoacetate → HCID 178432239, compound
Reaction equation
[F:1][C:2]([F:11])([F:10])[C:3]1[CH:9]=[CH:8][CH:7]=[CH:6][C:4]=1[NH2:5].[CH3:12][CH:13]([C:19](=O)[CH3:20])[C:14](OCC)=[O:15]>>[CH3:20][C:19]1[C:13]([CH3:12])=[C:14]([OH:15])[C:6]2[C:4](=[C:3]([C:2]([F:10])([F:11])[F:1])[CH:9]=[CH:8][CH:7]=2)[N:5]=1Participants
3
Procedure
Prepared according to procedure R using 2-(trifluoromethyl)aniline (1.61 g, 10 mmol) and ethyl 2-methyl-3-oxobutanoate (2.89 g, 20 mmol) in PPA (4 g, 40 mmol). The resulting precipitate was collected by filtration, washed with water, and dried to give 2,3-dimethyl-8-(trifluoromethyl)quinolin-4-ol. Mass Spectrum (ESI) m/e=242 (M+1).
Workup
- customPrepared
- filtrationThe resulting precipitate was collected by filtration
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-fb51ccdeec35494790c1662dec935cfd
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08765940B2
Reaction notes
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