HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(2,2-Dimethyl-5-oxo-[1,3]-dioxolan-4-ylidene)-n-methyl-n-(4-trifluoromethylbenzyl)-acetamide → 4-Hydroxy-1-(2-morpholin-4-yl-ethyl)-5-oxo-2,5-dihydro-1h-pyrrole-3-carboxylic acid methyl-(4-trifluoromethyl-benzyl)-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(2,2-Dimethyl-5-oxo-[1,3]-dioxolan-4-ylidene)-n-methyl-n-(4-trifluoromethylbenzyl)-acetamide | HCID 69655487 | — |
| Reactant | paraformaldehyde N-(2-aminoethyl)morpholine | HCID 86760256 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Hydroxy-1-(2-morpholin-4-yl-ethyl)-5-oxo-2,5-dihydro-1h-pyrrole-3-carboxylic acid methyl-(4-trifluoromethyl-benzyl)-amide | HCID 54704617 | 35% |
Reaction Steps
Reaction of 2-(2,2-dimethyl-5-oxo-[1,3]-dioxolan-4-ylidene)-N-methyl-N-(4-trifluoromethyl-benzyl)-acetamide (0.36 g, 1.05 mmol) with the paraformaldehyde-N-(2-aminoethyl)morpholine adduct in methanol using a procedure similar to the one described in the preparation of compound 13 gave 0.16 g (35% yield) of the title compound as a solid after chromatography on reversed phase silica gel. 1HNMR 400 MHz (CDCl3) δ (ppm); 2.46 (4H, m, 2×NCH2), 2.57 (2H, t, J=6.1 Hz, NCH2), 3.04 (3H, s, NCH3), 3.6 (6H, m, 2×OCH2 and NCH2), 4.25 (2H, s, NCH2), 4.72 (2H, s, NCH2), 7.41 (2H, d, J=8.0 Hz, aromatics), 7.62 (2H, d, J=8.0 Hz, aromatics). HRMS (FAB+) calculated for C20H25F3N3O4: [M+H]+: 428.179716. found: 428.179157.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07109186B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-a0b3a3d41d264302970023effa5dc9b0 |
| Source note | uspto-grants-2006_09 |