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HRID 2214957作成日:2026年10月25日

Sodium ethoxide → N-butyl-4-[7-chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridin-3-yl]-2-pyrimidinamine

https://huagongshe.com/reaction/2214957

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ethoxideHCID 2723922—
反応物1-[7-Chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridin-3-yl]-2-propyn-1-oneHCID 21948683—
反応物HCID 178449236HCID 178449236—
生成物N-butyl-4-[7-chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridin-3-yl]-2-pyrimidinamineHCID 2217484759%

反応手順

In a similar manner as described in Example 34 from 1-[7-chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridin-3-yl]-2-propyn-1-one (0.50 g, 1.7 mmol), N-butylguanidine sulfate and sodium ethoxide (0.81 mL, 21 wt % in ethanol, 2.2 mmol) at room temperature was obtained N-butyl-4-[7-chloro-2-(4-fluorophenyl)-pyrazolo[1,5-α]pyridin-3-yl]-2-pyrimidinamine (0.39 g, 59% o) as a fluffy pale yellow solid. 1H NMR (CDCl3): δ 8.40 (d, 1H), 8.07 (d, 1H), 7.65 (m, 2H), 7.29 (m, 1H), 7.15 (t, 2H), 7.06 (d, 1H), 6.32 (d, 1H), 5.16 (bs, 1H), 3.49 (q, 2H), 1.71–1.41 (m, 4H), 0.99 (t, 3H); 19F NMR (CDCl3) δ−112.77; MS m/z 396 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07109209B2
出典データセットuspto-grants-2006_09
ORD IDord-d0c724469e054bcd98bb5c77593ab006
出典メモuspto-grants-2006_09