HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(4-Chlorophenoxy)benzene-1-sulfonyl chloride → HCID 59467988, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(4-Chlorophenoxy)benzene-1-sulfonyl chloride | HCID 2757750 | — |
| Reactant | HCID 68518813 | HCID 68518813 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59467988 | HCID 59467988 | — |
Reaction Steps
To a suspension of (R)-3-amino-1-benzyloxy-piperidin-2-one hydrogen bromide salt (0.086 g, 0.29 mmol) (synthesized according to Miller's procedure J. Org. Chem. 2002, 67, 4759) and 4-(4-chloro-phenoxy)-benzenesulfonyl chloride (0.095 g, 0.31 mmol) in dry CH2Cl2 (3 mL) was treated with TEA (0.12 mL, 0.86 mmol) under N2. The reaction mixture was stirred at room temperature for 6 h and diluted with CH2Cl2 and water. After the usual work-up, the crude material was purified by chromatography (silica gel, 35% EtOAc/hexanes) to give the desired product, (R)—N-(1-Benzyloxy-2-oxo-piperidin-3-yl)-4-(4-chloro-phenoxy)-benzene-sulfonamide. MS (EI) 487 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07803793B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-d57a67655e1d4969859a57de19b38b08 |
| Source note | uspto-grants-2010_09 |