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HRID 732992作成日:2026年10月25日

5-amino-7-chloro-3-(2-fluorobenzyl)-3H-1,2,3-triazolo[4,5-d]pyrimidine → HCID 178508329、化合物

https://huagongshe.com/reaction/732992

反応式

関与物質

役割名称HCID仕込み量
反応物5-amino-7-chloro-3-(2-fluorobenzyl)-3H-1,2,3-triazolo[4,5-d]pyrimidineHCID 21874567—
反応物tributyl 1-(2-(trimethylsilyl)ethoxymethyl)-1H-triazol-5-ylstannaneHCID 68893656—
触媒HCID 178418476HCID 178418476—
溶媒DimethylformamideHCID 6228—
生成物HCID 178508329HCID 178508329—

反応条件

温度80 °C

反応手順

A mixture of 7-chloro-3-(2-fluorobenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine-5-amine (145 mg, 0.50 mmol), tributyl 1-(2-(trimethylsilyl)ethoxymethyl)-1H-triazol-5-ylstannane (336 mg, 0.75 mmol) and Pd(PPh3)2Cl2 (35 mg, 0.05 mmol) in DMF (2 mL) was shaken at 80° C. for 17 h then purified directly by chromatography [SiO2; iso-hexane:EtOAc (2:1)] to give 3-(2-fluorobenzyl)-7-(1-(2-trimethylsilyl)ethoxymethyl)-1H-triazol-5-yl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine-5-amine as a colourless oil. This material was dissolved in MeOH (1 mL), treated with a solution of HCl (0.5 mL, 4-M in dioxane), stirred for 17 h, concentrated in vacuo and the residue triturated with Et2O to give the title compound (16 mg, 10%) as an off-white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07589097B2
出典データセットuspto-grants-2009_09
ORD IDord-0ce9efba6d974369830ceba69adc500a
出典メモuspto-grants-2009_09