HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → tert-Butyl{(3S,5S,6R)-6-methyl-5-phenyl-2-[(4,4,4-trifluoro-2-hydroxybutyl)imino]piperidine-3-yl}carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Amino-4,4,4-trifluorobutan-2-ol hydrochloride | HCID 86238921 | — |
| Reactant | tert-Butyl[(3S,5S,6R)-6-methyl-5-phenyl-2-thioxopiperidin-3-yl]carbamate | HCID 131732078 | — |
| Catalyst | Mercuric Chloride | HCID 24085 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-Butyl{(3S,5S,6R)-6-methyl-5-phenyl-2-[(4,4,4-trifluoro-2-hydroxybutyl)imino]piperidine-3-yl}carbamate | HCID 137231131 | — |
Reaction Steps
To a solution of tert-butyl[(3S,5S,6R)-6-methyl-5-phenyl-2-thioxopiperidin-3-yl]carbamate (75 mg, 0.23 mmol) in ethanol (2.3 mL) was added 1-amino-4,4,4-trifluorobutan-2-ol hydrochloride (105 mg, 0.59 mmol), mercury(II) chloride (83 mg, 0.30 mmol), and triethylamine (78 μL, 0.56 mmol). The mixture was stirred 30 min, filtered, and then concentrated, giving the crude title compound. MS 430.3 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09067941B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-baedbb0cd2f94c47ac437184a04e63ca |
| Source note | uspto-grants-2015_06 |