Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium | HCID 5360545 | — |
| Edukt | 5-Iodo-6-methylpyrimidine-2,4-diamine | HCID 15855792 | — |
| Edukt | trans-3-Methyl-3-(4-trifluoromethylphenyl)-1-butenylboronic acid | HCID 21468004 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | HCID 21467991 | HCID 21467991 | 56,5% |
Reaktionsschritte
Sodium metal, 4.1 grams (0.18 mole), was stirred with 250 mL of ethanol for 30 minutes. After this time 20.0 grams (0.08 mole) of 2,4-diamino-5-iodo-6-methylpyrimidine (prepared in Step B of Example 3), 27.6 grams (0.11 mole) of trans-3-methyl-3-(4-trifluoromethylphenyl)-1-butenylboronic acid, and 9.2 grams (0.008 mole) of tetrakistriphenylphosphine palladium(0) were added. The reaction mixture was purged with nitrogen, and then heated to 80° C. where it stirred for about 28 hours. After this time the reaction mixture was concentrated under reduced pressure to about 20% of the original volume and then poured into 300 mL of water. The mixture was cooled in an ice-bath, and a solid was collected by filtration. The solid was triturated with a mixture of 1:1 petroleum ether:diethyl ether, and then subjected to column chromatography on silica gel using 5% methanol in methylene chloride as the eluant. The product-containing fractions were combined and concentrated under reduced pressure to a solid residue. The solid was recrystallized from 1-propanol and water, yielding 15.2 grams of trans-2,4-diamino-6-methyl-5-[3-(4-trifluoromethylphenyl)-3-methyl-1-butenyl]pyrimidine, mp 182°-185° C. The NMR spectrum was consistent with the proposed structure.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05622954 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-70aa6cbdaa024f8fb5516b67c593101f |
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| Quellennotiz | uspto-grants-1997_04 |
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