HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl p-toluenesulfonate →
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl p-toluenesulfonate | HCID 6645 | — |
| Reactant | HCID 606379 | HCID 606379 | — |
Reaction Steps
The title compound was prepared from 3-ethyl-5-(3-methyl-3H-benzothiazol-2-ylidene)-2-thioxothiazolidin-4-one and methyl p-toluenesulfonate in a manner similar to that described in Example 1. 1H-NMR (CDCl3): δ 7.82 (1H, d), 7.77 (2H, d), 7.58-7.66 (2H, m), 7.49 (1H, m), 7.08 (2H, d), 4.52 (3H, s), 4.21 (2H, q), 3.29 (3H, s), 2.29 (3H, s), 1.45 (3H, t).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06696473B2 |
| Source dataset | uspto-grants-2004_02 |
| ORD ID | ord-4fecb9975cd2487f98edddb26bbb7063 |
| Source note | uspto-grants-2004_02 |