HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 3168Erstellt: 24. Oktober 2026
Methylamine → Ethyl 4-(methylamino)-2-(methylsulfanyl)pyrimidine-5-carboxylate
https://huagongshe.com/de/reaction/3168
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methylamine | HCID 6329 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 4-Chloro-2-(methylthio)pyrimidine-5-carboxylic acid ethyl ester | HCID 80008 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | Ethyl 4-(methylamino)-2-(methylsulfanyl)pyrimidine-5-carboxylate | HCID 295697 | 81% |
Reaktionsschritte
To a solution of 4-chloro-2-methylsulfanyl-5-pyrimidinecarboxylate ethyl ester (18.66 g, 80.4 mmol) in 260 mL of tetrahydrofuran was added triethylamine (34 mL, 244 mmol), followed by 30 mL of a 40% aqueous solution of methylamine. The solution was stirred for 30 minutes at 25° C. then concentrated in vacuo and partitioned between chloroform and saturated aqueous sodium bicarbonate. The organic layer was washed with brine, dried over MgSO4, filtered, and concentrated to provide a white solid. The solid was suspended in hexane and filtered to provide 14.70 g (81%) of 4-methylamino-2-methylsulfanyl-5-pyrimidinecarboxylate ethyl ester; mp 91°-93° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05733914 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-dd5613fe644d4335b125576fcb33212e |
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| Quellennotiz | uspto-grants-1998_03 |
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