HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2S,3S)-(-)-3-tert-Butoxycarbonylamino-1,2-epoxy-4-phenylbutane → Trifluoroacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2S,3S)-(-)-3-tert-Butoxycarbonylamino-1,2-epoxy-4-phenylbutane | HCID 9903372 | — |
| Reactant | (4S)-6-bromo-2-methyl-2-(trifluoromethyl)chroman-4-amine | HCID 67305954 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 86614140 | HCID 86614140 | — |
Reaction Steps
A mixture of (4S)-6-bromo-2-methyl-2-(trifluoromethyl)chroman-4-amine (179 mg, 577 μmol) and tert-butyl (S)-1-((S)-oxiran-2-yl)-2-phenylethylcarbamate (198 mg, 750 μmol) in ethanol was heated at reflux for 16 h. At this point, there was still the starting amine left. An additional 1.3 eq of epoxide was added to the reaction, and continued to reflux for 6 h. The resulted mixture was concentrated and purified on Shimadzu HPLC to afford the title compound as a TFA salt. MS m/z: 573, 575.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745484B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-0737efb85022439ba9ec17ec97424d0a |
| Source note | uspto-grants-2010_06 |