HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Methoxide → N,N-diethyl 2-amino-4-methylthiazole-5-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | N,N-diethyl 2-acetamido-4-methylthiazole-5-sulfonamide | HCID 21850614 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | N,N-diethyl 2-amino-4-methylthiazole-5-sulfonamide | HCID 21850461 | 22.4% |
Reaction Conditions
| Temperature | 5 °C |
|---|
Reaction Steps
The product from Step 1 (2.5 g) was dissolved in methanol (25 cm3) and cooled to 5° C. with stirring under an atmosphere of nitrogen. Sodium methoxide in methanol (2 cm3 of 25% wt./vol. solution) was added dropwise and the mixture allowed to warm to the ambient temperature for 18 hours. The reaction was heated under reflux for 1 hour, cooled, diluted with water (250 cm3), extracted with diethyl ether (2×100 cm3), dried (MgSO4) and evaporated under reduced pressure to give N,N-diethyl 2-amino-4-methylthiazole-5-sulfonamide (0.48 g). M+ 249; 1H NMR: δ 1.20(6H,t); 2.48(3H,s); 3.28(4H,q); 5.25(2H,br s); (solid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05952359 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-cfa97ec3df174ccaa7ab27d05a8877b3 |
| Source note | uspto-grants-1999_09 |