HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ticlatone → 6-Chloro-3-oxo-3H-benzo[d]isothiazole-2-carboxylic acid propylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ticlatone | HCID 6258 | — |
| Reactant | Propyl isocyanate | HCID 61033 | — |
| Product | 6-Chloro-3-oxo-3H-benzo[d]isothiazole-2-carboxylic acid propylamide | HCID 11149920 | — |
Reaction Steps
Following the synthetic procedure of 6a as described in Example 1, compound 6u (96% yield) was synthesized from 6-chloro-benzo[d]isothiazol-3-one and n-propyl isocyanate as a white solid. IR(KBr) 3294, 1709, 1635, 1520 cm−1; 1H-NMR (CDCl3) δ1.00 (t, J=7.3 Hz, 3H), 1.61-1.71 (m, 2H), 3.38-3.44 (m, 2H), 7.38 (d, J=8.8 Hz, 1H), 7.58 (s, 1H), 7.93 (d, J=8.8 Hz, 1H), 8.79 (br s, 1H); ESIMS m/e 271 and 273 (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-50f4f6b7c43a439290ad02b749545df9 |
| Source note | uspto-grants-2009_09 |