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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 963433생성일: 2026년 10월 25일

Potassium Carbonate → 5-[3,4-Dimethoxy-5-(naphthalen-2-ylethynyl)-benzyl]-pyrimidine-2,4-diamine

https://huagongshe.com/reaction/963433

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물TriphenylphosphineHCID 11776—
반응물2-EthynylnaphthaleneHCID 115017—
반응물5-(3,4-Dimethoxy-5-iodo-benzyl)pyrimidine-2,4-diamineHCID 11101094—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물5-[3,4-Dimethoxy-5-(naphthalen-2-ylethynyl)-benzyl]-pyrimidine-2,4-diamineHCID 1908165858%

반응 단계

A mixture of 197 mg of 5-(3,4-dimethoxy-5-iodo-benzyl)pyrimidine-2,4-diamine, 155 mg of 2-ethynyl-naphthalene (Bull. Soc. Chim. Fr. [3], 7, 648, (1892)), 108 mg of potassium carbonate, 14 mg of triphenylphosphine and 5 mg of copper(I) iodide in 2 ml of dimethylformamide is heated at 100° for 4 hrs. The reaction mixture is cooled to room temperature, poured into 50 ml of water and extracted three times with 50 ml of methylene chloride each time. The organic phases are washed with 50 ml of water, dried over magnesium sulphate and concentrated. The crude product is recrystallized from ethyl acetate/n-hexane. 121 mg (58%) of 5-[3,4-dimethoxy-5-(naphthalen-2-ylethynyl)-benzyl]-pyrimidine-2,4-diamine are obtained as a yellowish solid. M.p. 152°-155°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05763450
출처 데이터셋uspto-grants-1998_06
ORD IDord-2cdae77e1559449aab36177774fa590d
출처 메모uspto-grants-1998_06