HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl p-toluenesulfonate → 2-bromo-4-(N-methylacetamido)thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl p-toluenesulfonate | HCID 6645 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Acetamido-2-bromo-thiazole | HCID 20294043 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-bromo-4-(N-methylacetamido)thiazole | HCID 20377168 | 32% |
Reaction Steps
A solution of 4-acetamido-2-bromothiazole and methyl tosylate (4.65 g, 25 mM) in dry acetonitrile (125 ml) was treated with a 60% dispersion of sodium hydride in oil (1 g, 25 mM) and the mixture stirred 72 hours at ambient temperature. The reaction mixture was filtered and the filtrate evaporated under reduced pressure. The residue was chromatographed on silica (Woelm grade 1, 150 g) using 2% methanol in chloroform as eluant. Evaporations of the appropriate fractions followed by recrystallisation from hexane gave 2-bromo-4-(N-methylacetamido)thiazole (1.9 g, 32%) mp 84° C. Found: C, 30.55; H, 2.95; N, 11.8%, C6H7N2BrOS requires C, 30.7; H, 3.0; N, 11.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04105773 |
| Source dataset | uspto-grants-1978_08 |
| ORD ID | ord-0e6177a085d14aae9e36264aadc3c510 |
| Source note | uspto-grants-1978_08 |