Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 13290240 | HCID 13290240 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13290252 | HCID 13290252 | 61.4% |
Reaction Steps
Over five hours, at a temperature of -30° C., a solution of 9.28 g (0.127 mole) of diethylamine and 12.84 g (0.127 mole) of triethylamine in 80 ml of tetrahydrofuran was added dropwise to a solution of 40.0 g (0.121 mole) of 6-(4-chloro-N-ethylanilino)-2,4-dichloro-pyrimidine-5-carbaldehyde in 400 ml of tetrahydrofuran. The solution was then stirred for four hours at -30° C. and for two hours at 20° C., the triethylammoniumchloride was filtered off, and the filtrate evaporated in vacuo. After the filtrate was mixed by stirring with 120 ml of diethylether, 27.3 g of colorless crystals were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04619885 |
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| Source dataset | uspto-grants-1986_10 |
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| ORD ID | ord-ea5dbaa1e3304d6387d2ee5809f1ffd0 |
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| Source note | uspto-grants-1986_10 |
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