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HRID 8299作成日:2026年10月24日

Thiazole → 1-(2-Fluorobenzyl)-4-(2-thiazolyl)-1H-pyrazolo[3,4-d]pyrimidine-6-amine

https://huagongshe.com/ja/reaction/8299

反応式

関与物質

役割名称HCID仕込み量
反応物ThiazoleHCID 9256—
反応物4-chloro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-d]pyrimidine-6-amineHCID 22015505—
反応物ButyllithiumHCID 178418339—
触媒ZincchlorideHCID 3007855—
触媒HCID 178418397HCID 178418397—
溶媒TetrahydrofuranHCID 8028—
溶媒Ammonium ChlorideHCID 25517—
生成物1-(2-Fluorobenzyl)-4-(2-thiazolyl)-1H-pyrazolo[3,4-d]pyrimidine-6-amineHCID 22015509—

反応手順

A stirred solution of thiazole (0.14 mL, 2 mmol) in dry THF (10 mL) at −78° C., under argon was treated n-BuLi (1.6-M in hexanes, 1.25 mL, 2 mmol), stirred for 15 min, treated with ZnCl2 solution (1-M in Et2O, 2 mL, 2 mmol) then allowed to warm gradually to room temperature. The mixture was treated with 4-chloro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-d]pyrimidine-6-amine (278 mg, 1 mmol) and Pd(PPh3)4 (100 mg, 10 mol %), refluxed for 2 h, diluted with saturated NH4Cl solution, extracted with EtOAc, dried (MgSO4) and concentrated in vacuo. The resulting brown oil was purified by chromatography [SiO2; heptane:EtOAc (4:1) then (3:1)] to give the title compund (101 mg, 31%) as a cream solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087754B2
出典データセットuspto-grants-2006_08
ORD IDord-cbb1bf1895cf4e479b2fbd67b4d61173
出典メモuspto-grants-2006_08