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HRID 1038839作成日:2026年10月25日

Potassium Carbonate → HCID 68751488、化合物

https://huagongshe.com/reaction/1038839

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4-(Methylsulfonyl)anilineHCID 79617—
反応物2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
反応物2-chloro-N-cyclopropylfuro[3,2-d]pyrimidin-4-amineHCID 86665093—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒tert-ButanolHCID 6386—
生成物HCID 68751488HCID 6875148827.8%

反応条件

温度100 °C

反応手順

A vial was charged with 2-chloro-N-cyclopropylfuro[3,2-d]pyrimidin-4-amine (0.09 g, 0.429 mmol, Preparation #A.1), 4-(methylsulfonyl)aniline (0.077 g, 0.451 mmol, Oakwood), X-Phos (0.020 g, 0.043 mmol), Pd2dba3 (0.020 g, 0.021 mmol), K2CO3 (0.062 g, 0.451 mmol) and t-BuOH (3.5 mL). The vial was purged with argon and heated at about 100° C. overnight. The mixture was diluted with CHCl3 (about 10 mL) passed through a SiCO3 SPE cartridge and concentrated. The crude product was purified by preparative reverse phase HPLC (Table 2, Method a) to provide N4-allyl-N2-(4-(methylsulfonyl)phenyl)furo[3,2-d]pyrimidine-2,4-diamine (0.041 g, 27%): 1H NMR (DMSO-d6) δ 9.53 (s, 1H), 8.11 (d, J=2.1 Hz, 1H), 8.02 (m, 3H), 7.72 (d, J=8.9 Hz, 2H), 6.80 (d, J=2.1 Hz, 1H), 6.00 (ddd, J=17.1, 10.2, 5.1 Hz, 1H), 5.22 (dd, J=17.1, 1.6 Hz, 1H), 5.11 (dd, J=10.5, 1.6 Hz, 1H), 4.14 (dd, J=5.1 Hz, 2H), 3.11 (s, 3H). Syk IC50=B.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08551981B2
出典データセットuspto-grants-2013_10
ORD IDord-073ca5a0a38f4c1599ce3e0d5c1fe0e7
出典メモuspto-grants-2013_10