HCID 178469292, compound → HCID 178481168, compound
Reaction equation
C([O:3][C:4]([C:6]1[N:11]([CH3:12])[C:10]2[CH:13]=[C:14]([Br:20])[C:15](=[O:19])[C:16]([OH:18])=[CH:17][C:9]=2[C:8](=[O:21])[CH:7]=1)=[O:5])C>Cl>[Br:20][C:14]1[C:15](=[O:19])[C:16]([OH:18])=[CH:17][C:9]2[C:8](=[O:21])[CH:7]=[C:6]([C:4]([OH:5])=[O:3])[N:11]([CH3:12])[C:10]=2[CH:13]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 4,7-dihydro-8-bromo-4,7-dioxo-6-hydroxy-1-methyl-1H-cyclohepta[b]pyridine-2-carboxylic acid ethyl ester (3.6 g, described in Example 9) and concentrated hydrochloric acid (300 ml) is refluxed for 30 min and cooled to room temperature. The precipitate is collected and washed with water to give the title compound, mp > 250° C.
Workup
- temperatureis refluxed for 30 min
- customThe precipitate is collected
- washwashed with water
Sources & evidence
- ORD record
- ord-2c7964dc2ef74433b34863216ad3564c
- Source dataset
- uspto-grants-1978_12
- Patent number
- US04130649
Reaction notes
Loading…