HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,5-Difluorobenzyl bromide → HCID 10274932, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,5-Difluorobenzyl bromide | HCID 518896 | — |
| Reactant | HCID 10267727 | HCID 10267727 | — |
| Product | HCID 10274932 | HCID 10274932 | 85% |
Reaction Steps
The title compound is prepared in a manner analogous to the procedure set forth in Example 48 from 3,5-difluorobenzyl bromide and [2-hydroxy-2-(4-hydroxyphenyl)cyclohexyl][(methylethyl)sulfonyl]amine to provide 511 mg as a brown oil. This material was purified via silica gel chromatography employing the Chromatotron® using a 4000 micron rotor while eluting with a solvent of methylene chloride/ethyl acetate 4:1 to yield the title compound (360 mg, 85%) as a white solid. Ion spray M.S. 438.3 (M*−1). Calculated for C22H27NO4SF2: Theory: C 60.12, H 6.19, N 3.19. Found: C 59.32, H 6.14, N 3.26.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06900353B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-7d846c00df79496e80c12b08872d4236 |
| Source note | uspto-grants-2005_05 |