HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thioacetamide → Methyl 2-methyl-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thioacetamide | HCID 2723949 | — |
| Reactant | HCID 83646766 | HCID 83646766 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methyl 2-methyl-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxylate | HCID 90303556 | — |
Reaction Steps
A soln. of methyl 2-bromo-3-oxocyclohexanecarboxylate (150 mg, 0.64 mmol) and thioacetamide (53 mg, 0.70 mmol) in EtOH (3 mL) was stirred at 85° C. overnight. Subsequently, the mixture was quenched with aq. sat. NaHCO3 and extracted with EtOAc. The comb. org. layers were washed with brine, dried over MgSO4, and conc. in vacuo. Purification by means of CC (0-40% EtOAc/Hept) provided a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09388197B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-ec4bd327b123450fbabae25352b1e6e8 |
| Source note | uspto-grants-2016_07 |