HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ticlatone → 6-Chloro-3-oxo-3H-benzo[d]isothiazole-2-carboxylic acid butylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ticlatone | HCID 6258 | — |
| Reactant | Butyl isocyanate | HCID 8110 | — |
| Product | 6-Chloro-3-oxo-3H-benzo[d]isothiazole-2-carboxylic acid butylamide | HCID 11266104 | — |
Reaction Steps
Following the synthetic procedure of 6a as described in Example 1, compound 6w (90% yield) was synthesized from 6-chloro-benzo[d]isothiazol-3-one and n-butyl isocyanate as a white solid. IR(CHCl3) 3294, 1713, 1540 cm−1; 1H-NMR (DMSO-d6) δ0.89 (t, J=7.3 Hz, 3H), 1.26-1.37 (m, 2H), 1.47-1.55 (m, 2H), 3.28-3.34 (m, 2H), 7.50 (d, J=8.3 Hz, 1H), 7.91 (d, J=8.3 Hz, 1H), 8.14 (s, 1H), 8.76 (t, J=5.6 Hz, 1H); ESIMS m/e 284 and 286 (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-74c3c2c81b064d77869cadd39e71f29b |
| Source note | uspto-grants-2009_09 |