HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl (3R,6S)-6-(2,3-difluorophenyl)-2-thioxoazepan-3-ylcarbamate → HCID 178453870, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl (3R,6S)-6-(2,3-difluorophenyl)-2-thioxoazepan-3-ylcarbamate | HCID 59734935 | — |
| Reactant | 2-Amino-1-[1-(trifluoromethyl)cyclopropyl]ethanol | HCID 67525848 | — |
| Catalyst | Mercuric Chloride | HCID 24085 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178453870 | HCID 178453870 | — |
Reaction Steps
Mercury(II) chloride (149 mg, 0.547 mmol) was added to a solution of tert-butyl [(3R,6S)-6-(2,3-difluorophenyl)-2-thioxoazepan-3-yl]carbamate (150 mg, 0.421 mmol, described in Intermediate 7), and 2-amino-1-[1-(trifluoromethyl)cyclopropyl]ethanol (569 mg, 3.367 mmol) in ethanol (5 mL) at 60° C. After 10 min, the reaction was allowed to cool to ambient temperature. The mixture was filtered and concentrated under reduced pressure. Saturated aqueous NaHCO3 was added and the mixture was extracted with CH2Cl2 (3×). The combined organic extracts were dried over MgSO4, filtered, and concentrated under reduced pressure to give the title compound. MS: m/z=492 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08993588B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-68740388d3404200bdf3059f9846546c |
| Source note | uspto-grants-2015_03 |