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HRID 3425作成日:2026年10月23日

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/ja/reaction/3425

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfamic AcidHCID 5987—
反応物1-(3-Aminopropyl)-4-methylpiperazineHCID 78328—
反応物Sodium BicarbonateHCID 516892—
反応物6-(2,6-Dichlorophenyl)pyrido[2,3-d]pyrimidine-2,7-diamineHCID 5328113—
溶媒WaterHCID 962—
生成物6-(2,6-dichlorophenyl)-2-N-[3-(4-methylpiperazin-1-yl)propyl]pyrido[2,3-d]pyrimidine-2,7-diamineHCID 5328148—

反応条件

温度150 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05733913
出典データセットuspto-grants-1998_03
ORD IDord-9674881c08004af9ba181216cc7781b2
出典メモuspto-grants-1998_03