HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinimide → 5-Amino-4-iodo-3-methyl-1-(2,4,6-trichlorophenyl)pyrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 3-Methyl-1-(2,4,6-trichlorophenyl)-1H-pyrazol-5-amine | HCID 2060032 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Amino-4-iodo-3-methyl-1-(2,4,6-trichlorophenyl)pyrazole | HCID 18780720 | — |
Reaction Steps
A stirred solution of 5-amino-3-methyl-1-(2,4,6-trichlorophenyl)pyrazole (WO-A-94/13643; 35 g) and N-iodosuccinimide (29 g) in acetonitrile (450 ml) was heated under reflux for 1.5 hours, then the reaction mixture allowed to cool and evaporated under reduced pressure. The residue was dissolved in dichloromethane and the solution washed successively with aqueous sodium thiosulphate solution, water and brine, then dried (Na2SO4) and evaporated under reduced pressure. The resulting dark coloured solid was triturated with hexane to yield the title compound as a pale orange solid, m.p. 135-137° C. δ(CDCl3): 2.25 (s,3H), 3.67 (br.s,2H), 7.49 (s,2H). MS (thermospray): M/Z [M+H] 401.4; C10H7Cl3 lN3 +H requires 401.88.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06075043 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-d239e1a860f941579e3fa5b60df0d72e |
| Source note | uspto-grants-2000_06 |