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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3232생성일: 2026년 10월 24일

Triethylamine → Pyrido[2,3-d]pyrimidin-7-one deriv. 13

https://huagongshe.com/ko/reaction/3232

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium hydrideHCID 24758—
반응물4-(Chloromethyl)pyridinium chlorideHCID 74570—
반응물SodiumHCID 5360545—
반응물2-Amino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidin-7-olHCID 10494915—
용매DimethylformamideHCID 6228—
생성물Pyrido[2,3-d]pyrimidin-7-one deriv. 13HCID 5328633—

반응 조건

온도70 °C

반응 단계

To a suspension of NaH (60% in mineral oil, 32 mg) in 6 mL of dimethylformamide was added 2-amino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidin-7(8H)-one (200 mg, 0.65 mmol) and the mixture heated to 70° C. In a second flask containing triethyl amine (220 μL, 1.59 mmol) in 4 mL of dimethylformamide was added 4-picolyl chloride hydrochloride (137 mg, 0.84 mmol). This dark red mixture was added to the above solution of the sodium salt of 2-amino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidin-7(8H)-one. The mixture was heated to 70° C., then cooled to room temperature. The mixture was poured into 20 mL of ice water, and the resulting precipitate was removed by filtration and washed with water. This solid was washed with 10% methanol in ethyl acetate to provide 96 mg of crude product. The filtrate was concentrated to provide an additional 77 mg of crude product. An analytical sample was obtained by purification by flash chromatography, eluting with a gradient of ethyl acetate to 10% methanol in ethyl acetate to provide 2-amino-6-(2,6-dichlorophenyl)-8-pyridin-4-ylmethyl-8H-pyrido[2,3-d]pyrimidin-7-one; mp 268°-270° C. dec.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733914
출처 데이터셋uspto-grants-1998_03
ORD IDord-d68719fd07424782a508df3f799b02af
출처 메모uspto-grants-1998_03