HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 4-methyl-2-(2-oxo-3-phenylimidazolidin-1-yl)thiazole-5-carboxylate → 4-Methyl-2-(2-oxo-3-(3-phenylpropyl)imidazolidin-1-yl)thiazole-5-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 4-methyl-2-(2-oxo-3-phenylimidazolidin-1-yl)thiazole-5-carboxylate | HCID 58031446 | — |
| Reactant | Ethyl 4-methyl-2-(2-oxo-3-(3-phenylpropyl)imidazolidin-1-yl)thiazole-5-carboxylate | HCID 58031520 | — |
| Product | 4-Methyl-2-(2-oxo-3-(3-phenylpropyl)imidazolidin-1-yl)thiazole-5-carboxylic acid | HCID 58031464 | 99% |
Reaction Steps
Following the procedure as described in Example 6, making variations as required to replace ethyl 4-methyl-2-(2-oxo-3-phenylimidazolidin-1-yl)thiazole-5-carboxylate with ethyl 4-methyl-2-(2-oxo-3-(3-phenylpropyl)imidazolidin-1-yl)thiazole-5-carboxylate, the title compound was obtained in 99% yield: mp 218-221° C.; 1H NMR (300 MHz, DMSO-d6) δ 7.25-7.10 (m, 5H), 3.94-3.89 (m, 2H), 3.53-3.48 (m, 2H), 3.22 (t, J=6.9 Hz, 2H), 2.55 (t, J=7.5 Hz, 2H), 2.46 (s, 3H), 1.83-1.73 (m, 2H); MS (ES+) m/z 346.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063084B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-a2d21c38323948259e0781742237db83 |
| Source note | uspto-grants-2011_11 |