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HRID 1963940作成日:2026年10月25日

6-(5-chloro-2-fluoropyridin-4-yl)-5-methyl-N-((tetrahydro-2H-pyran-4-yl)methyl) pyrazin-2-amine → HCID 178432953、化合物

https://huagongshe.com/reaction/1963940

反応式

関与物質

役割名称HCID仕込み量
反応物6-(5-chloro-2-fluoropyridin-4-yl)-5-methyl-N-((tetrahydro-2H-pyran-4-yl)methyl) pyrazin-2-amineHCID 66936875—
反応物HCID 178511674HCID 178511674—
溶媒Dimethyl SulfoxideHCID 679—
生成物HCID 178432953HCID 1784329539.71%

反応条件

温度100 °C

反応手順

To a scintillation vial containing 6-(5-chloro-2-fluoropyridin-4-yl)-5-methyl-N-((tetrahydro-2H-pyran-4-yl)methyl)pyrazin-2-amine (7 mg, 0.021 mmol) was added DMSO and trans-cyclohexane-1,4-diamine (23.73 mg, 0.208 mmol). The homogenous reaction mixture was capped and heated to 100° C. in an oil bath for 4 hr. The crude solution was purified by reverse phase preparative HPLC to yield trans-N1-(5-chloro-4-(3-methyl-6-((tetrahydro-2H-pyran-4-yl)methyl)aminopyrazin-2-yl)pyridin-2-yl)cyclohexane-1,4-diamine (1.1 mg, 2.018 μmol, 9.71% yield), LCMS (m/z): 431.2 (MH+), retention time=0.47 min as a TFA salt after lyophilizing.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08415381B2
出典データセットuspto-grants-2013_04
ORD IDord-faa0822f6355421c8d053e009f52de59
出典メモuspto-grants-2013_04