HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)- → methyl N-{(4-bromophenyl)[4-(methylsulfonyl)phenyl]methylene}leucinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)- | HCID 18462 | — |
| Reactant | Leucine methyl ester hydrochloride | HCID 2723695 | — |
| Reactant | (4-Bromophenyl)(4-(methylsulfonyl)phenyl)methanone | HCID 21262853 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | methyl N-{(4-bromophenyl)[4-(methylsulfonyl)phenyl]methylene}leucinate | HCID 86590539 | — |
Reaction Steps
A solution of (4-bromophenyl)[4-(methylsulfonyl)phenyl]methanone (202 mg, 0.59 mmol), L-leucine methyl ester hydrochloride (328 mg, 2.0 mmol) and camphor sulfonic acid (52 mg, 0.22 mmol) in toluene was refluxed for 18 hours using a Dean-Stark trap. The solvent was removed in vacuo and the resulting residue was purified by chromatography using EtOAc and hexane as eluant to give a 1:1 mixture of the title compound and the starting (4-bromophenyl)[4-(methylsulfonyl)phenyl]methanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07973037B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-1d1a031a40bc4066b6a7e2b45349c06d |
| Source note | uspto-grants-2011_07 |