戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 963433作成日:2026年10月26日

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

https://huagongshe.com/reaction/963433

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物TriphenylphosphineHCID 11776—
反応物2-EthynylnaphthaleneHCID 115017—
反応物5-(3,4-Dimethoxy-5-iodo-benzyl)pyrimidine-2,4-diamineHCID 11101094—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物5-[3,4-Dimethoxy-5-(naphthalen-2-ylethynyl)-benzyl]-pyrimidine-2,4-diamineHCID 1908165858%

反応手順

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°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05763450
出典データセットuspto-grants-1998_06
ORD IDord-2cdae77e1559449aab36177774fa590d
出典メモuspto-grants-1998_06