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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3425생성일: 2026년 10월 23일

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/ko/reaction/3425

반응식

참여 물질

역할이름HCID투입량
반응물Sulfamic AcidHCID 5987—
반응물1-(3-Aminopropyl)-4-methylpiperazineHCID 78328—
반응물Sodium BicarbonateHCID 516892—
반응물6-(2,6-Dichlorophenyl)pyrido[2,3-d]pyrimidine-2,7-diamineHCID 5328113—
용매WaterHCID 962—
생성물6-(2,6-dichlorophenyl)-2-N-[3-(4-methylpiperazin-1-yl)propyl]pyrido[2,3-d]pyrimidine-2,7-diamineHCID 5328148—

반응 조건

온도150 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733913
출처 데이터셋uspto-grants-1998_03
ORD IDord-9674881c08004af9ba181216cc7781b2
출처 메모uspto-grants-1998_03