Sodium Hydroxide → HCID 15157756, compound
Reaction equation
[C:1]([C:4]1[CH:5]=[C:6]2[C:11](=[C:12]([C:14]([OH:16])=[O:15])[CH:13]=1)[NH:10][CH2:9][CH2:8][CH:7]2[C:17]([OH:19])=[O:18])(=[O:3])N.[OH-:20].[Na+]>>[NH:10]1[C:11]2[C:6](=[CH:5][C:4]([C:1]([OH:20])=[O:3])=[CH:13][C:12]=2[C:14]([OH:16])=[O:15])[CH:7]([C:17]([OH:19])=[O:18])[CH2:8][CH2:9]1Participants
3
Procedure
A solution of 6-carbamoyl-1,2,3,4-tetrahydroquinoline-4,8-dicarboxylic acid (1.77 g) in 10% aqueous sodium hydroxide solution (20 ml) was refluxed for 10 hours and after cooling, adjusted to pH 1. The resulting precipitate was collected by filtration, washed with water and dried to give the title compound (1.29 g, 72.9%) which was recrystallized from ethanol to white crystals, mp 240° C.-241° C.
Workup
- temperatureafter cooling, adjusted to pH 1
- filtrationThe resulting precipitate was collected by filtration
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-555e5492978b4f79b2efc735fa7c67a4
- Source dataset
- uspto-grants-1992_05
- Patent number
- US05112836
Reaction notes
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