HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 4-cyano-N-methoxymethyl-N-thiazol-2-yl-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Acetyl-n-(thiazol-2-yl)benzenesulfonamide | HCID 21082529 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-cyano-N-methoxymethyl-N-thiazol-2-yl-benzenesulfonamide | HCID 67001447 | — |
Reaction Steps
To a suspension of 4-acetyl-N-thiazol-2-yl-benzenesulfonamide (10 mmol) and potassium carbonate (15 mmol) in DMF (30 mL) was added chloro-methoxy-methane (10 mmol) and the mixture was stirred for 4 h. The reaction mixture was diluted with water (30 mL) and the resulting mixture was extracted with ethyl acetate. The organic phase was washed with brine, dried over MgSO4, and concentrated in vacuo. The crude product was purified by column chromatography to give 4-cyano-N-methoxymethyl-N-thiazol-2-yl-benzenesulfonamide (5.2 mmol) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063080B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-bd905ec12b7c40eaac587f50a0bdb360 |
| Source note | uspto-grants-2011_11 |