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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 617935Generated: November 1, 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/reaction/617935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfamic AcidHCID 5987—
Reactant1-(3-Aminopropyl)-4-methylpiperazineHCID 78328—
ReactantSodium BicarbonateHCID 516892—
Reactant6-(2,6-Dichlorophenyl)pyrido[2,3-d]pyrimidine-2,7-diamineHCID 5328113—
SolventWaterHCID 962—
Product6-(2,6-dichlorophenyl)-2-N-[3-(4-methylpiperazin-1-yl)propyl]pyrido[2,3-d]pyrimidine-2,7-diamineHCID 5328148—

Reaction Conditions

Temperature150 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05952342
Source datasetuspto-grants-1999_09
ORD IDord-b4d656816fb6437298dbf6354b7675c2
Source noteuspto-grants-1999_09