Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloropyrimidine-4-carboxamide | HCID 247028 | — |
| Reactant | HCID 54522065 | HCID 54522065 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15233812 | HCID 15233812 | — |
Reaction Steps
3.0 g (7.45 mmol) of N-(2-aminoethyl)-2-[[3-[[2-(2-methoxyphenoxy) ethyl]methylamino]propyl]amino]-pyrimidine-4-carboxamide, 1.23 g (7.8 mmol) of 2-chloropyrimidine-4-carboxamide, 1.55 g (11.2 mmol) of potassiumcarbonate and 0.1 g of sodium iodide are introduced into 40 ml of N,N-dimethylformamide in a 0.25 l, three-necked, round-bottomed flask and the reaction mixture is heated at 60° C. for 15 h. The mixture is cooled to room temperature and the reaction product is poured onto 100 ml of water and extracted with ethyl acetate (3×100 ml). The organic phase is washed with water, dried over sodium sulphate, filtered and the solvents are evaporated under reduced pressure. After recrystallisation from ethyl acetate, 1.95 g of compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05330985 |
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| Source dataset | uspto-grants-1994_07 |
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| ORD ID | ord-d0b566d4e50d46bbba745133b89476a9 |
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| Source note | uspto-grants-1994_07 |
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