Hydrochloric Acid → HCID 21422148, compound
Reaction equation
[N:1]1[CH:6]=[C:5]([NH:7][C:8](=[O:14])[C:9]([O:11]CC)=[O:10])[CH:4]=[CH:3][C:2]=1[NH:15][C:16](=[O:22])[C:17]([O:19]CC)=[O:18].Cl>[OH-].[Na+].O>[N:1]1[CH:6]=[C:5]([NH:7][C:8](=[O:14])[C:9]([OH:11])=[O:10])[CH:4]=[CH:3][C:2]=1[NH:15][C:16](=[O:22])[C:17]([OH:19])=[O:18]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Diethyl N,N'-2,5-pyridinediyldioxamate (1.0 g., 0.0032 mole) is stirred in 1.0N sodium hydroxide (25 ml.) at 70°-85° until solution is complete. The reaction mixture is diluted with water (25 ml.) and acidified (pH=3) with concentrated hydrochloric acid. The desired product is collected by filtration (0.35 g., 43%, m.p. 290°-295° dec.).
Workup
- filtrationThe desired product is collected by filtration (0.35 g., 43%, m.p. 290°-295° dec.)
Sources & evidence
- ORD record
- ord-6875d8c13dbd44509643ce78236a17ec
- Source dataset
- uspto-grants-1976_06
- Patent number
- US03963660
Reaction notes
Loading…