HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methyl-2-methylthioquinolinium p-toluenesulfonate → 2-(5-acetyl-2-ethylaminophenylimino)-3-benzyl-5-(1-methyl-1H-quinolin-2-ylidene)thiazolidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methyl-2-methylthioquinolinium p-toluenesulfonate | HCID 15597093 | — |
| Reactant | 2-(5-Acetyl-2-ethylaminophenylimino)-3-benzylthiazolidin-4-one | HCID 21937583 | — |
| Product | 2-(5-acetyl-2-ethylaminophenylimino)-3-benzyl-5-(1-methyl-1H-quinolin-2-ylidene)thiazolidin-4-one | HCID 73855092 | — |
Reaction Steps
In a manner similar to Example 102, 1-methyl-2-methylthioquinolinium p-toluenesulfonate was condensed with 2-(5-acetyl-2-ethylaminophenylimino)-3-benzylthiazolidin-4-one to afford the title compound. 1H-NMR (CDCl3): δ 7.66–7.71 (2H, m), 7.43–7.56 (4H, m), 7.20–7.38 (7H, m), 6.53 (1H, d), 5.20 (2H, s), 3.78 (3H, br s), 3.07 (2H, q), 2.51 (3H, s), 1.06 (3H, t); MS(ESI): 509 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115640B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-a528a83930f0468281bd716cb8e843ef |
| Source note | uspto-grants-2006_10 |