HuagongsheHuagongshe Chemistry Print Report · For research reference only
Mci-186 → 1-Phenyl-3-methyl-4-(3,4-dichlorophenylcarbamoyl)-2-pyrazolin-5-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Mci-186 | HCID 4021 | — |
| Reactant | 3,4-Dichlorophenyl isocyanate | HCID 7607 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triethylammonium | HCID 1385867 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1-Phenyl-3-methyl-4-(3,4-dichlorophenylcarbamoyl)-2-pyrazolin-5-one | HCID 20335439 | — |
Reaction Steps
The solution of 13 g of 1-phenyl-3-methyl-2-pyrazolin-5-one in 150 ml of benzene and 9.1 g of triethylamine is combined at ambient temperature with the solution of 14.0 g of 3,4-dichlorophenylisocyanate in the minimum amount of benzene. The triethylammonium salt separates after 2 hours standing at room temperature and the mixture is evaporated. The residue is poured into 0.3 N hydrochloric acid, the solid collected, washed with water, dried, triturated with cold methanol and recrystallized from ethyl acetate to yield the 1-phenyl-3-methyl-4-(3,4-dichlorophenylcarbamoyl)-2-pyrazolin-5-one of Formula II with R=H, R'=3--Cl and R"=Cl, melting at 228°-231° (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04207317 |
| Source dataset | uspto-grants-1980_06 |
| ORD ID | ord-4bdbca9fc0164fb2956e6412e6ca482b |
| Source note | uspto-grants-1980_06 |