Sodium Carbonate → HCID 10704722, compound
Reaction equation
[N+]([C:4]1[CH:11]=[C:10]([C:12]#[N:13])[CH:9]=[CH:8][C:5]=1[C:6]#[N:7])([O-])=O.[C:14]([O:18][CH3:19])(=[O:17])[CH2:15][SH:16].C([O-])([O-])=O.[Na+].[Na+]>CO>[NH2:7][C:6]1[C:5]2[CH:8]=[CH:9][C:10]([C:12]#[N:13])=[CH:11][C:4]=2[S:16][C:15]=1[C:14]([O:18][CH3:19])=[O:17]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Nitroterephthalonitrile (5.0 g, 28.9 mmol), prepared by the method of Gorvin, U.S. Pat. No. 4,250,182, was treated with 1 equivalent methyl thioglycolate and 1 equivalent Na2CO3 in methanol by the prcx:edure described in Example 41A to yield the title compound (5.50 g, 82%). 1H NMR (300 MHz, DMSO) δ 8.50 (s, 1H), 8.32 (d, 1H), 7.80 (dd, 1H), 7.29 (br s, 2H), 3.81 (s, 3H). MS (DCI/NH3) m/e 250 (M+NH4)+.
Sources & evidence
- ORD record
- ord-c0e7e33288ca4f30bddd527b3acdbd14
- Source dataset
- uspto-grants-1997_01
- Patent number
- US05597823
Reaction notes
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