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HRID 709933作成日:2026年10月27日

Dimethylformamide → 4-Chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carbaldehyde

https://huagongshe.com/reaction/709933

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidineHCID 5380710—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物4-Chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carbaldehydeHCID 56763828—

反応条件

温度-78 °C

反応手順

To a solution of 5-bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine (E-2) (2.33 g, 10.0 mmol, 1.0 eq) in anhydrous THF (100 mL) at −78° C. under argon, n-BuLi solution (2.5 M in THF, 8.8 mL, 22.0 mmol, 2.2 eq) is added dropwise (over 10 min). The resulting mixture is stirred at −78° C. for 1 h and then DMF (2.0 g, 11.0 mmol, 1.1 eq) is added dropwise (over 10 min). The mixture is stirred at −78° C. for an additional 30 min and then stirred at RT overnight. The reaction mixture is quenched with H2O (50 mL) and then concentrated in vacuo. The residue is triturated with saturated aqueous NH4Cl solution. The solid is collected by filtration, rinsed with ethyl acetate, and dried in vacuo to afford the product, 4-chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carbaldehyde (E-3).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181221B2
出典データセットuspto-grants-2015_11
ORD IDord-a83455aca6fc4d6499d8a051de35a8bc
出典メモuspto-grants-2015_11