HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → HCID 10361797, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 10450038 | HCID 10450038 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 10361797 | HCID 10361797 | 45% |
| Product | HCID 10430981 | HCID 10430981 | 27% |
Reaction Steps
Diisopropylethylamine (407 μL, 2.34 mmol) and ethyl iodine (187 μL, 2.34 mmol) were added to a solution of 6-amino-2-(4-fluoro-phenyl)-5-isopropoxy-benzofuran-3-carboxylic acid methylamide, prepared according to Example 16 (200 mg, 584 μmol) in dry acetonitrile (8 mL). The reaction was monitored under analytical LC/MS conditions and quenched by addition of water (4 mL). After concentration to dryness, the crude product was purified by preparative HPLC (reverse phase C18, acetonitrile/water plus 0.1% acetic acid), affording 97 mg (45%) of the 6-ethylamino-2-(4-fluoro-phenyl)-5-isopropoxy-benzofuran-3-carboxylic acid methylamide and 63 mg (27%) of 6-diethylamino-2-(4-fluoro-phenyl)-5-isopropoxy-benzofuran-3-carboxylic acid methylamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07666863B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-4f5ca5088e284fa3897e6b4b55d26fce |
| Source note | uspto-grants-2010_02 |