HCID 86590075, compound → HCID 18752895, compound
Reaction equation
[NH2:1][C:2]1[C:7](/[CH:8]=[CH:9]/[C:10]([O:12]C(C)(C)C)=[O:11])=[CH:6][C:5]([Cl:17])=[CH:4][N:3]=1>FC(F)(F)C(O)=O.C1(C)C=CC=CC=1>[NH2:1][C:2]1[C:7](/[CH:8]=[CH:9]/[C:10]([OH:12])=[O:11])=[CH:6][C:5]([Cl:17])=[CH:4][N:3]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
t-Butyl (E)-3-(2-amino-5-chloro-3-pyridinyl)-2-propenoate (2 g, 7.8 mmol), was stirred in 3 ml of trifluoroacetic acid at ambient temperature for 1 hour. The reaction mixture was diluted with toluene, evaporated to dryness, and the residue triturated with diethyl ether to yield the title compound as a pale yellow solid (1.89 g, 6.0 mmol).
Workup
- customevaporated to dryness
- customthe residue triturated with diethyl ether
Sources & evidence
- ORD record
- ord-efc579d9a2384d328dcbac1bbe79eb46
- Source dataset
- uspto-grants-2003_06
- Patent number
- US06583162B1
Reaction notes
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