HuagongsheHuagongshe Chemistry Print Report · For research reference only
alpha-(Aminomethyl)-2,2-dimethyl-1,3-dioxolane-4-methanol → 2-[N-(4-Fluoro-3-trifluoromethylphenyl)sulfamoyl] acetic acid-[2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)-ethylamide]
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | alpha-(Aminomethyl)-2,2-dimethyl-1,3-dioxolane-4-methanol | HCID 11971028 | — |
| Reactant | 2-[N-(4-fluoro-3-trifluoromethylphenyl)sulfamoyl]acetic acid | HCID 19764008 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-[N-(4-Fluoro-3-trifluoromethylphenyl)sulfamoyl] acetic acid-[2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)-ethylamide] | HCID 67899691 | — |
Reaction Steps
Analogously to the instructions for Example 9(a), 2.21 g (7 mmol) of 2-[N-(4-fluoro-3-trifluoromethyl-phenyl)sulfamoyl] acetic acid in dioxane is reacted with 1.13 g (7 mmol) of 2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)-ethylamine for about 1 hour at 90° C. After concentration by evaporation and crystallization from ethanol/ether, 2.87 g=92.3% of the theoretical yield is obtained as a crystallizate. Melting point 144°-146° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05130119 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-d5f814d27334473d87ebcdc33b9e8a41 |
| Source note | uspto-grants-1992_07 |