HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → tert-Butyl{(3S,5S,6R)-2-[(2-hydroxy-3-methoxy-3-methylbutyl)imino]-6-methyl-5-phenylpiperidin-3-yl}carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Amino-3-methoxy-3-methylbutan-2-ol | HCID 55285086 | — |
| 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)-2-[(2-hydroxy-3-methoxy-3-methylbutyl)imino]-6-methyl-5-phenylpiperidin-3-yl}carbamate | HCID 137187577 | — |
Reaction Steps
To a solution of tert-butyl[(3S,5S,6R)-6-methyl-5-phenyl-2-thioxopiperidin-3-yl]carbamate (150 mg, 0.47 mmol) in ethanol (4.7 mL) was added 1-amino-3-methoxy-3-methylbutan-2-ol (156 mg, 1.17 mmol), mercury (II) chloride (165 mg, 0.61 mmol), and triethylamine (163 μL, 1.17 mmol). The mixture was stirred 20 min, and then concentrated, giving the crude title compound. MS 420.4 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895572B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-a3e45ccfceb946e8a893cac88bb13f32 |
| Source note | uspto-grants-2014_11 |