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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29818Erstellt: 24. Oktober 2026

Methylamine → 2-chloro-N-methyl-5-nitropyrimidin-4-amine

https://huagongshe.com/de/reaction/29818

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethylamineHCID 6329—
Edukt2,4-Dichloro-5-nitropyrimidineHCID 521266—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-chloro-N-methyl-5-nitropyrimidin-4-amineHCID 714723299,3%

Reaktionsschritte

A solution of 2,4-dichloro-5-nitropyrimidine (7.26 g, 37.4 mmol) in THF (100 ml) is cooled to −78° C. A solution of methyl amine (8 M in methanol, 9.35 mL, 74.8 mmol) is added dropwise. The mixture is allowed to warm to room temperature, and concentrated. The residue is partitioned between ethyl acetate and water. The layer is separated and the aqueous layer is extracted with ethyl acetate. The combined organic extracts are washed with brine, dried over Na2SO4, filtered and concentrated to afford the title product (7.0 g). (Note: the product contains 5% regio-isomer, 4-chloro-2-(methylamino)-5-nitropyrimidine). The residue is used in the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07423038B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-83d91350d3d04fa4bc5182a219334930
Quellennotizuspto-grants-2008_09