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HRID 732991作成日:2026年10月25日

Tetrahydrofuran → 3-(2-Fluorobenzyl)-7-(5-oxazolyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine-5-amine

https://huagongshe.com/reaction/732991

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物OxazoleHCID 9255—
反応物5-amino-7-chloro-3-(2-fluorobenzyl)-3H-1,2,3-triazolo[4,5-d]pyrimidineHCID 21874567—
反応物ButyllithiumHCID 178418339—
触媒ZincchlorideHCID 3007855—
触媒HCID 178418397HCID 178418397—
生成物3-(2-Fluorobenzyl)-7-(5-oxazolyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine-5-amineHCID 218745592%
生成物Isohexane ethyl acetateHCID 21882781—

反応手順

A stirred solution of oxazole (138 mg, 2.0 mmol) in dry THF (10 mL) at −78° C., under argon was treated with n-BuLi (1.25 mL, 1.6-M in hexanes, 2.0 mmol), stirred for 30 min, treated with a solution of ZnCl2 (2.0 mL, 1-M in Et2O, 2.0 mmol)) and allowed to warm gradually to room temperature. The mixture was treated with 7-chloro-3-(2-fluorobenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine-5-amine (280 mg, 1.0 mmol) and Pd(PPh3)4 (100 mg), refluxed for 4 h and partitioned between saturated NH4Cl solution (10 mL) and EtOAc (10 mL). The organic phase was dried (MgSO4), concentrated in vacuo and purified by chromatography [SiO2; iso-hexane:EtOAc (1:1), then neat EtOAc] to give the title compound (6 mg, 2%) as a beige 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-dbee5352534544369fe8b93c50159921
出典メモuspto-grants-2009_09