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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 617949생성일: 2026년 10월 24일

Sulfamic Acid → 6-(2,6-dichlorophenyl)-2-N-[4-(diethylamino)butyl]pyrido[2,3-d]pyrimidine-2,7-diamine

https://huagongshe.com/ko/reaction/617949

반응식

참여 물질

역할이름HCID투입량
반응물Sulfamic AcidHCID 5987—
반응물N,N-Diethyl-1,4-butanediamineHCID 117976—
반응물6-(2,6-Dichlorophenyl)pyrido[2,3-d]pyrimidine-2,7-diamineHCID 5328113—
생성물6-(2,6-dichlorophenyl)-2-N-[4-(diethylamino)butyl]pyrido[2,3-d]pyrimidine-2,7-diamineHCID 5328133—

반응 조건

온도150 °C

반응 단계

A mixture of 2,7-diamino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidine (40 g) from Example 1, sulfamic acid (25.4 g) and diethylaminobutylamine (205 mL) was heated to approximately 150° C. for 28 hours. The reaction temperature was lowered to 50° C., and excess diethylaminobutylamine was removed in vacuo. After cooling to 25° C., the residue was suspended 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, washed several times, first with a saturated solution of sodium bicarbonate then a saturated solution of sodium chloride, dried over magnesium sulfate and concentrated in vacuo. The residue was washed repeatedly with diethyl ether and then crystallized from ethyl acetate. The recrystallized product was further purified by column chromatography, eluting first with ethyl acetate:methyl alcohol:triethylamine (85:14:1) followed by ethyl acetate:ethyl alcohol:triethylamine (9:2:1) to afford 36.2 g of the title compound 6-(2,6-dichlorophenyl)-N2 -(4-diethylamino-butyl)-pyrido[2,3-d]pyrimidine-2,7-diamine, CIMS (1% N3 in CH4): 461=M+ +C2H5, 433=M+ +H (Base), 417, 403, 360.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05952342
출처 데이터셋uspto-grants-1999_09
ORD IDord-3bdc5d55884c47c4ac67a97f78fd03f9
출처 메모uspto-grants-1999_09