HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-[2-(2-Methyl-4-pentylphenoxy)ethylamino]thieno[2,3-d]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Chlorothieno[2,3-d]pyrimidine | HCID 736618 | — |
| Reactant | 2-(2-Methyl-4-pentylphenoxy)ethylamine | HCID 15588031 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-[2-(2-Methyl-4-pentylphenoxy)ethylamino]thieno[2,3-d]pyrimidine | HCID 13343190 | 76% |
Reaction Steps
3.4 g (0.02 mole) of 4-chlorothieno[2,3-d]pyrimidine, 4.4 g (0.02 mole) of 2-(2-methyl-4-pentylphenoxy)ethylamine and 2 g (0.02 mole) of triethylamine were dissolved in 50 ml of toluene, and the solution was heated under reflux for 4 hours. At the end of this time, water was added to the reaction mixture, and the mixture was then extracted with toluene. The extract was dried over anhydrous sodium sulphate, and the solvent was distilled off, after which the residue was recrystallised from a mixture of toluene and hexane, to give 5.4 g (yield 76%) of the title compound in the form of colourless crystals melting at 93°-95° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04562193 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-0ae162c335404a32b5759b13682389a7 |
| Source note | uspto-grants-1985_12 |