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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 890251생성일: 2026년 10월 26일

Ethanol → N,N'-bis(4-amino-2-methyl-6-quinolyl)-2,4-diamino-6-chloro-5-methylsulfanyl-pyrimidine

https://huagongshe.com/reaction/890251

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물2-Methylquinoline-4,6-diamineHCID 223995—
반응물N-(4-amino-2-methyl-6-quinolyl)-2-amino-4,6-dichloro-5-methylsulfanylpyrimidineHCID 22250299—
생성물N,N'-bis(4-amino-2-methyl-6-quinolyl)-2,4-diamino-6-chloro-5-methylsulfanyl-pyrimidineHCID 69588754—

반응 단계

A mixture of 43 mg of N-(4-amino-2-methyl-6-quinolyl)-2-amino-4,6-dichloro-5-methylsulfanylpyrimidine and 55 mg of 4,6-diamino-2-methylquinoline in 5 mL of ethanol is heated under reflux for about 3 hours, left at a temperature in the region of 20° C. for about 16 hours and then filtered. The filtrate is concentrated under reduced pressure (2.7 kPa) at a temperature in the region of 40° C., and then the residue obtained is purified by HPLC (column: C18 Waters, 5 M, 50×19 mm; eluent: elution gradient water-acetonitrile-TFA (0.07%) from 95-5 to 5-95 over 30 minutes). The fractions containing the desired product are combined and concentrated to dryness under reduced pressure (2.7 kPa) at a temperature in the region of 40° C. to obtain 12 mg of N,N′-bis(4-amino-2-methyl-6-quinolyl)-2,4-diamino-6-chloro-5-methylsulfanyl-pyrimidine in the form of a beige colored solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06995175B2
출처 데이터셋uspto-grants-2006_02
ORD IDord-9bf56a2bfb094f739b344600036807a4
출처 메모uspto-grants-2006_02