HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ticlatone → 6-Chloro-3-oxo-3H-benzo[d]isothiazole-2-carboxylic acid benzylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ticlatone | HCID 6258 | — |
| Reactant | Benzyl isocyanate | HCID 76639 | — |
| Product | 6-Chloro-3-oxo-3H-benzo[d]isothiazole-2-carboxylic acid benzylamide | HCID 11162947 | — |
Reaction Steps
Following the synthetic procedure of 6a as described in Example 1, compound 6z (95% yield) was synthesized from 6-chloro-benzo[d]isothiazol-3-one and benzyl isocyanate as a white solid. IR(CHCl3) 3289, 1713, 1536 cm−1; 1H-NMR (CDCl3) δ4.63 (d, J=5.8 Hz, 2H), 7.22-7.40 (m, 6H), 7.58 (s, 1H), 7.92 (d, J=8.8 Hz, 1H), 9.15 (br s, 1H); ESIMS m/e 319 and 321 (M++1, 35Cl and 37Cl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07595403B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-a44ee70c91e14c60aa20e05e7743720b |
| Source note | uspto-grants-2009_09 |