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HRID 2069893作成日:2026年10月26日

Potassium Carbonate → 1-(6-(2-Butynyloxy)pyrimidin-4-yl)-cis-2,6-dimethylhexahydroazepine

https://huagongshe.com/reaction/2069893

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2-Butyn-1-olHCID 12991—
反応物4,6-DifluoropyrimidineHCID 137717—
反応物cis-2,6-DimethylhexahydroazepineHCID 66594949—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒TriethylamineHCID 8471—
生成物1-(6-(2-Butynyloxy)pyrimidin-4-yl)-cis-2,6-dimethylhexahydroazepineHCID 66594955—

反応条件

温度30 °C

反応手順

To a mixture obtained by adding 110.0 g of 4,6-difluoropyrimidine, 132.3 g of potassium carbonate and 19.2 g of triethylamine to 220.0 g of toluene, 69.8 g of 2-butyn-1-ol is added dropwise at 25 to 30° C. over one hour, followed by stirring at 30° C. Then, 220.0 g of water is added dropwise into the reaction mixture, followed by stirring. Then, 126.6 g of cis-2,6-dimethylhexahydroazepine is added dropwise and, after the mixture is stirred at 30° C., the reaction mixture is allowed to stand. After separating into the organic layer and the aqueous layer, the aqueous layer is removed and the organic layer is washed once with 220.0 g of 5% hydrochloric acid and then washed once with 220.0 g of water. The organic layer is concentrated to obtain 1-(6-(2-butynyloxy)pyrimidin-4-yl)-cis-2,6-dimethylhexahydroazepine (hereinafter referred to as the present compound (4)).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08299245B2
出典データセットuspto-grants-2012_10
ORD IDord-be5bc849d89a4e97890072fc0fcff32a
出典メモuspto-grants-2012_10