HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl p-toluenesulfonate → HCID 74052868, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl p-toluenesulfonate | HCID 6645 | — |
| Reactant | HCID 21937426 | HCID 21937426 | — |
| Reactant | HCID 73855039 | HCID 73855039 | — |
| Product | HCID 74052868 | HCID 74052868 | — |
Reaction Steps
Likewise as described in Example 1, intermediate 3′-benzyl-3,5-dimethyl-4-phenyl-2′-thioxo-2′,3′-dihydro-3H-[2,5′]bithiazolyliden-4′-one was alkylated with methyl p-toluenesulfonate and condensed with N-(3-amino-4-ethylaminophenyl)-2-methoxyacetamide to afford the title compound. 1H-NMR (CDCl3): δ 8.00 (1H, br s), 7.42-7.51 (5H, m), 7.30-7.37 (3H, m), 7.19-7.26 (3H, m), 7.11 (1H, d), 6.53 (1H, br s), 5.18 (2H, s), 3.97 (2H, s), 3.47 (3H, s), 3.42 (3H, s), 2.98 (2H, m), 2.06 (3H, s), 1.02 (3H, br t); MS(ESI): 600 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06696473B2 |
| Source dataset | uspto-grants-2004_02 |
| ORD ID | ord-add108fcdd544506bcfaf0fc9a454bf3 |
| Source note | uspto-grants-2004_02 |