HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → N-(2-trimethylammonioethyl)-6-methyl-4-(3-nitrophenyl)-2-phenyl-5-pyrimidinecarboxamide iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | N-(2-dimethylaminoethyl)-6-methyl-4-(3-nitrophenyl)-2-phenyl-5-pyrimidinecarboxamide | HCID 10319094 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(2-trimethylammonioethyl)-6-methyl-4-(3-nitrophenyl)-2-phenyl-5-pyrimidinecarboxamide iodide | HCID 20183398 | — |
Reaction Steps
A solution of N-(2-dimethylaminoethyl)-6-methyl-4-(3-nitrophenyl)-2-phenyl-5-pyrimidinecarboxamide (1 g) and methyl iodide (10.46 ml) in ethyl acetate (2 ml) was stirred for 5 days at room temperature. The reaction mixture was evaporated and the residue was recrystallized from ethyl alcohol to afford N-(2-trimethylammonioethyl)-6-methyl-4-(3-nitrophenyl)-2-phenyl-5-pyrimidinecarboxamide iodide (0.95 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04698340 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-5145226ba38e43da8288f99e534ed148 |
| Source note | uspto-grants-1987_10 |