HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiophenol → Ethyl 2-(4-(benzo[d]thiazol-2-yl)-2-methoxyphenoxy)-2-methylpropanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | Ethyl 2-(4-formyl-2-methoxyphenoxy)-2-methylpropanoate | HCID 71497692 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 2-(4-(benzo[d]thiazol-2-yl)-2-methoxyphenoxy)-2-methylpropanoate | HCID 68279194 | 93% |
Reaction Steps
In a DMF (3 mL) solvent in the presence of Na2S2O5 (136.1 mg, 0.71 mmol), a solution including Compound 122a (188.7 mg, 0.71 mmol) and 2-aminothiophenol (0.08 mL, 0.71 mmol) was stirred at room temperature for 2 days. After DMF was evaporated, the residual was distributed between ethyl acetate and water. An organic layer was dried, filtered, and evaporated. The residual was purified by silica gel column chromatography using hexane and ethyl acetate (EtOAc) (7:1) to obtain Compound 122b (244.8 mg, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08889881B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-f58376a8940e47ecac92d44e90b8da97 |
| Source note | uspto-grants-2014_11 |