Hydrochloric Acid → HCID 10431897, compound
Reaction equation
[CH3:1][N:2]([CH2:12][CH2:13][S:14][C:15]1[CH:28]=[CH:27][C:18]([CH:19]=[C:20]2[S:24][C:23](=[O:25])[NH:22][C:21]2=[O:26])=[CH:17][CH:16]=1)[C:3]1[O:4][C:5]2[CH:11]=[CH:10][CH:9]=[CH:8][C:6]=2[N:7]=1.[Mg].Cl.C([O-])(O)=O.[Na+]>CO.O1CCOCC1.O>[CH3:1][N:2]([CH2:12][CH2:13][S:14][C:15]1[CH:16]=[CH:17][C:18]([CH2:19][CH:20]2[S:24][C:23](=[O:25])[NH:22][C:21]2=[O:26])=[CH:27][CH:28]=1)[C:3]1[O:4][C:5]2[CH:11]=[CH:10][CH:9]=[CH:8][C:6]=2[N:7]=1Participants
8
Procedure
5-(4-[2-(N-Methyl-N-(2-benzoxazolyl)amino)ethylthio]-benzylidene)-2,4-thiazolidinedione (2 g) was dissolved in a mixture of methanol (70 ml) and 1,4-dioxan (70 ml). Magnesium turnings (1.7 g) were added and the solution stirred until no more effervescence was observed. The mixture was added to water (300 ml), acidified (2M HCl) to form a solution, neutralised (saturated NaHCO3 solution) and extracted with dichloromethane (3×150 ml). The organic extracts were washed with brine
Workup
- customto form a solution
- extractionextracted with dichloromethane (3×150 ml)
- washThe organic extracts were washed with brine
Sources & evidence
- ORD record
- ord-0263135cdad64605b7ab90670fd5e825
- Source dataset
- uspto-grants-1991_12
- Patent number
- US05075300
Reaction notes
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