Hydrochloric Acid → HCID 178524590, compound
Reaction equation
C([O:3][C:4]([C:6]1[NH:11][C:10]2[CH:12]=[CH:13][C:14](=[O:18])[C:15]([OH:17])=[CH:16][C:9]=2[C:8](=[O:19])[CH:7]=1)=[O:5])C.Cl>>[O:19]=[C:8]1[CH:7]=[C:6]([C:4]([OH:5])=[O:3])[NH:11][C:10]2[CH:12]=[CH:13][C:14](=[O:18])[C:15]([OH:17])=[CH:16][C:9]1=2Participants
3
Procedure
A mixture of 4,7-dihydro-4,7-dioxo-6-hydroxy-1H-cyclohepta[b]pyridine-2-carboxylic acid ethyl ester (2.5 g, described in Example 3) and 19% hydrochloric acid (75 ml) is refluxed for 1 hour and cooled to room temperature. The crystalline precipitate is collected and washed with water, ethanol and ether to obtain the title compound, mp > 270° C.
Workup
- temperatureis refluxed for 1 hour
- customThe crystalline precipitate is collected
- washwashed with water, ethanol and ether
Sources & evidence
- ORD record
- ord-78a56da359094e41b40b68c9b96d18ea
- Source dataset
- uspto-grants-1978_12
- Patent number
- US04130649
Reaction notes
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