HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Top-1288
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenyl 5-tert-butyl-2-methoxy-3-(methylsulfonamido)phenylcarbamate | HCID 86275692 | — |
| Reactant | HCID 117598555 | HCID 117598555 | — |
| Solvent | Isopropyl Acetate | HCID 7915 | — |
| Product | Top-1288 | HCID 81689783 | — |
Reaction Steps
A stirred mixture of phenyl(5-(tert-butyl)-2-methoxy-3-(methylsulfonamido)phenyl)-carbamate (see step 1(vii) above; 95 mg, 0.239 mmol), the product from step (vi) above (120 mg, 0.217 mmol) and Et3N (6 μL, 0.043 mmol) in i-PrOAc (3 mL) was heated at 70° C. overnight. The reaction was cooled to rt and concentrated in vacuo. The remainder was purified by chromatography on silica gel (40 g column, 0-5% MeOH in EtOAc) to afford an oil, which was triturated with diethyl ether to afford a light beige solid. The crude product was purified by preparative HPLC (Varian, Basic (10 mM Ammonium Bicarbonate), Waters X-Bridge Prep-C18, 5 μm, 19×50 mm column, 35-70% MeCN in Water) to afford the title compound (69 mg) as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08927563B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-031175c58c3b4c999e169d65f27e31f5 |
| Source note | uspto-grants-2015_01 |