Ammonia → HCID 19843277, compound
Reaction equation
[CH2:1]([O:3][C:4]1[C:8]2[N:9]([CH3:19])[CH:10]=[C:11]([C:14](OCC)=[O:15])[C:12](=[O:13])[C:7]=2[S:6][CH:5]=1)[CH3:2].[NH3:20]>C(O)C>[CH2:1]([O:3][C:4]1[C:8]2[N:9]([CH3:19])[CH:10]=[C:11]([C:14]([NH2:20])=[O:15])[C:12](=[O:13])[C:7]=2[S:6][CH:5]=1)[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Ethyl 3-ethoxy-4-methyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxylate (3 g) and a saturated solution of ammonia in ethanol (70 ml) were stirred together in a sealed stainless steel pressure vessel at 130° for 24 hours. After allowing to cool to ambient temperature the mixture was filtered and the solid was dried to give the novel compound 3-ethoxy-4-methyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide, m.p. 286°-287°.
Workup
- filtrationwas filtered
- customthe solid was dried
Sources & evidence
- ORD record
- ord-06e020972fb74e07874b2f79de65feec
- Source dataset
- uspto-grants-1989_10
- Patent number
- US04877793
Reaction notes
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