HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 20368183, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | Phosphorus trifluoride | HCID 62665 | — |
| Reactant | HCID 20368169 | HCID 20368169 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20368183 | HCID 20368183 | — |
Reaction Steps
The preparation of a 5-amino-1-(haloalkyl)-3-(1-methyl-5-nitro-2-imidazolyl)pyrazole-4-carbonitrile is accomplished by reacting the corresponding hydroxyalkyl compound with a halogenating agent such as phosphorus trichloride, phosphorus tribromide, phosphorus trifluoride, thionyl chloride and the like. Thus, 5-amino-1-(β-hydroxyethyl)-3-(1-methyl-5-nitro-2-imidazolyl)pyrazole-4-carbonitrile is allowed to react with thionyl chloride in an inert solvent such as benzene, in the presence of a small amount of dimethylformamide to yield 5-amino-1-(β-chloroethyl)-3-(1-methyl-5-nitro-2-imidazolyl)pyrazole-4-carbonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04075222 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-9d1624ca685e4316ad15a83408e3c4e9 |
| Source note | uspto-grants-1978_02 |