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CAS No. : | 556-90-1 | MDL No. : | MFCD00003186 |
Formula : | C3H4N2OS | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | - |
M.W : | 116.14 | Pubchem ID : | - |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H302-H315-H319-H335 | Packing Group: | |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
54% | General procedure: To the magnetically stirred solution of 17 (232 mg, 2 mmol) in HOAc (7 mL), was added NaOAc (500 mg, 6 mmol). After 15 min 3,4-dimethoxybenzaldhyde (16a, 400 mg, 2.4 mmol) was added and the reaction mixture was heated under reflux for 72 h. The HOAc was removed under reduced pressure and the resultant solid was washed successively with water, methanol and EtOAc to obtain the desired products as solid. 10.2.1.6 5-(4-Methoxy-3-nitrobenzylidene)-2-iminothiazolidin-4-one (14f) Orange solid; mp > 200 C; 301 mg, 54% yield; IR (neat) νmax = 3236, 2951, 1682, 1608 cm-1; 1H NMR (400 MHz, CD3SOCD3) δ 9.49 (s, 1H), 9.21 (s, 1H), 8.11 (s, 1H), 7.86 (d, J = 8.00 1H), 7.58 (s, 1H) 7.51 (d, J = 8.84, 1H) 4.31 (s, 3H); 13C NMR (100 MHz, CD3SOCD3): δ 180.62, 175.61, 153.00, 139.71, 135.70, 130.05, 127.13, 125.98, 115.70, 57.51: HRMS (ESI-TOF): m/z calculated for C11H9N3O4S [M+Na]+, 302.0211; found 302.0244. |
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