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HRID 3425Erstellt: 23. Oktober 2026

Sulfamic Acid → 6-(2,6-dichlorophenyl)-2-N-[3-(4-methylpiperazin-1-yl)propyl]pyrido[2,3-d]pyrimidine-2,7-diamine

https://huagongshe.com/de/reaction/3425

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfamic AcidHCID 5987—
Edukt1-(3-Aminopropyl)-4-methylpiperazineHCID 78328—
EduktSodium BicarbonateHCID 516892—
Edukt6-(2,6-Dichlorophenyl)pyrido[2,3-d]pyrimidine-2,7-diamineHCID 5328113—
LösungsmittelWaterHCID 962—
Produkt6-(2,6-dichlorophenyl)-2-N-[3-(4-methylpiperazin-1-yl)propyl]pyrido[2,3-d]pyrimidine-2,7-diamineHCID 5328148—

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

A mixture of 2,7-diamino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidine (3.0 g) from Example 1, sulfamic acid (1.9 g), and 1-(3-aminopropyl)-4-methylpiperazine (15 mL) was heated to approximately 150° C. for 24 hours. After cooling, the residue was dissolved in water. The aqueous solution was made alkaline with a solution of saturated sodium bicarbonate and extracted with dichloromethane several times. The dichloromethane layers were combined, dried over magnesium sulfate, and concentrated in vacuo. The residue was recrystallized from ethyl acetate to give 2.0 g of 6-(2,6-dichlorophenyl)-N2 -[3-(4-methyl-piperazin-1-yl)-propyl]-pyrido[2,3-d]pyrimidine-2,7-diamine, CIMS (1% NH3 in CH4): 474=M+ +C2H5, 446=M+ +H (Base); mp 208°-211° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05733913
Quelldatensatzuspto-grants-1998_03
ORD IDord-9674881c08004af9ba181216cc7781b2
Quellennotizuspto-grants-1998_03