Hydrochloric Acid → HCID 135705351, compound
Reaction equation
C([O:3][C:4](=[O:25])[CH2:5][N:6]1[C:11]([C:12]([O:14]CC)=[O:13])=[CH:10][C:9](=[O:17])[C:8]2[CH:18]=[C:19]([OH:24])[C:20](=[O:23])C=C[C:7]1=2)C.[OH-].[K+].Cl>>[C:12]([C:11]1[N:6]([CH2:5][C:4]([OH:3])=[O:25])[C:7]2[C:20](=[O:23])[C:19]([OH:24])=[CH:18][C:8]=2[C:9](=[O:17])[CH:10]=1)([OH:14])=[O:13]Participants
4
Procedure
A mixture of 4,7-dihydro-4,7-dioxo-2-ethoxycarbonyl-6-hydroxy-1H-cyclohepta[b]pyridine-1-acetic acid ethyl ester (1.7 g, described in Example 15) and 1N potassium hydroxide (12 ml) is stirred at room temperature for 2.5 hr. Hydrochloric acid (19%) is added until the mixture is acidic. The precipitate is collected and washed with water, acetone and ether to obtain the title compound, mp > 270° C.
Workup
- customThe precipitate is collected
- washwashed with water, acetone and ether
Sources & evidence
- ORD record
- ord-f723d5965d3f4062bb18159442e11eae
- Source dataset
- uspto-grants-1978_12
- Patent number
- US04130649
Reaction notes
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