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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3443생성일: 2026년 10월 24일

Sodium hydride → 3-Tert-butyl-1-[6-(2,6-dichlorophenyl)-2-{[3-(morpholin-4-yl)propyl]amino}pyrido[2,3-d]pyrimidin-7-yl]urea

https://huagongshe.com/ko/reaction/3443

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물tert-Butyl isocyanateHCID 62412—
반응물6-Arylpyrido[2,3-d]pyrimidine deriv. 42HCID 5328144—
용매DimethylformamideHCID 6228—
생성물3-Tert-butyl-1-[6-(2,6-dichlorophenyl)-2-{[3-(morpholin-4-yl)propyl]amino}pyrido[2,3-d]pyrimidin-7-yl]ureaHCID 532814579.8%

반응 단계

To a solution of 6-(2,6-dichlorophenyl)-N2 -(3-morpholin-4-yl-propyl)-pyrido[2,3-d]pyrimidine-2,7-diamine (1.0 g) from Example 58 in DMF (15 mL) was added one equivalent of 60% sodium hydride suspension (0.92 g). After stirring for approximately 1 hour at room temperature, one equivalent of tert-butyl isocyanate (0.230 g) was added, and the reaction was monitored by thin layer chromatography. After approximately 4 hours, the solvent was removed in vacuo. The residue was partitioned between ethyl acetate and water. The aqueous layer was washed several times with ethyl acetate. The ethyl acetate layers were combined, dried with magnesium sulfate, and concentrated in vacuo. Chromatography of the residue on silica gel using ethyl acetate followed by ethyl acetate:ethanol:triethylamine (18:2:1) gave 0.98 g of the title compound 1-tert-butyl-3-[6-(2,6-dichlorophenyl)-2-(3-morpholin-4-yl-propylamino)-pyrido[2,3-d]pyrimidin-7-yl]-urea, CIMS (1% NH3 in CH4): 532=M+ +H, 531=M+,433, 84 (Base); mp 236°-240° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733913
출처 데이터셋uspto-grants-1998_03
ORD IDord-ede167eccc134bd3a388eacac4ece473
출처 메모uspto-grants-1998_03