HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Xylene → N-(5-(1-(4-Acetoxytetrahydrofuran-3-yloxycarbonyl)ethylamino)-4-chloro-2-fluorophenyl)-3,4,5,6-tetrahydrophthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-(3-amino-4-chloro-6-fluorophenyl)-3,4,5,6-tetrahydrophthalimide | HCID 15590180 | — |
| Reactant | 4-Acetoxytetrahydrofuran-3-yl 2-bromopropionate | HCID 20078949 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(5-(1-(4-Acetoxytetrahydrofuran-3-yloxycarbonyl)ethylamino)-4-chloro-2-fluorophenyl)-3,4,5,6-tetrahydrophthalimide | HCID 20078935 | 32.9% |
Reaction Steps
A mixture of 8.84 g of N-(5-amino-4-chloro-2-fluorophenyl)-3,4,5,6-tetrahydrophthalimide, 12.6 g of 4-acetoxytetrahydrofuran-3-yl 2-bromopropionate, 3.02 g of sodium hydrogencarbonate and 3 ml of xylene was heated under stirring at 150° to 160 ° C. for 4 hours. Adding ethyl acetate to the reaction mixture while it remained warm, the resulting mixture was washed with water, subsequently with aqueous saturated sodium chloride solution, and dried over anhydrous magnesium sulfate. After distilling off the solvent, the residue was purified by chromatography on a silica gel column (development solvent: ethyl acetate/hexane=1/2), to obtain 4.88 g of a compound described in Table 1 (No. 10) (33%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05405828 |
| Source dataset | uspto-grants-1995_04 |
| ORD ID | ord-653fee0bc36d4b6ba4be69ed5419edd7 |
| Source note | uspto-grants-1995_04 |