HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → E-1210
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Di-tert-butyl (3-(3-(4-((pyridin-2-yloxy)methyl)benzyl)isoxazol-5-yl)pyridin-2-yl)imidodicarbonate | HCID 25114167 | — |
| Reactant | Sodium bicarbonate water | HCID 86585896 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | E-1210 | HCID 16719049 | — |
Reaction Steps
To a solution of di-tert-butyl(3-(3-(4-((pyridin-2-yloxy)methyl)benzyl)isoxazol-5-yl)pyridin-2-yl)imidodicarbonate described in Preparation Example 3-1-2 (11.8 g, purity approximately 70%) and dichloromethane (120 mL) was added trifluoroacetic acid (40 mL) at 0° C. Stirring was carried out at room temperature for 14 hours. To the reaction solution was added saturated sodium bicarbonate water at 20° C or lower, extracted with ethyl acetate, and then purified by NH-silica gel column chromatography (heptane:ethyl acetate=1:1). The solvent was concentrated under a reduced pressure, tert-butyl methyl ether was added to the resulting residue, and solids were filtered to obtain the title compound (7.29 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08058444B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-b87a6374a89e4dac8b9ad0babfdc99b0 |
| Source note | uspto-grants-2011_11 |