HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formamide → Methyl 4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formamide | HCID 713 | — |
| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | HCID 83646766 | HCID 83646766 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl 4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxylate | HCID 90303216 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
At 0° C., finely crushed P4S10 (9.35 g, 21.0 mmol) was added to a mixture of formamide (4.73 g, 105.0 mmol) in dioxane (28.5 mL). Subsequently, the mixture was stirred in a sealed vial at 100° C. for 1.5 h, cooled to RT and filtrated. The filtrate was added to a mixture of methyl 2-bromo-3-oxocyclohexanecarboxylate (2.06 g, 8.76 mmol) in dioxane (16.5 mL) and stirred in a sealed vial at 80° C. overnight. The mixture was quenched by the addition of 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 (10-40% 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-8be6ff8a724c4742808a0d1c8404842b |
| Source note | uspto-grants-2016_07 |