戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 270704作成日:2026年10月25日

Hydrochloric Acid → 4-Amino-2-(methylsulfanyl)pyrimidine-5-carbaldehyde

https://huagongshe.com/reaction/270704

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium CarbonateHCID 10340—
反応物4-Amino-2-(methylsulfanyl)pyrimidine-5-carbonitrileHCID 295757—
反応物DiisobutylaluminumhydrideHCID 21225700—
溶媒TetrahydrofuranHCID 8028—
生成物4-Amino-2-(methylsulfanyl)pyrimidine-5-carbaldehydeHCID 29576953.1%

反応条件

温度0 °C

反応手順

To a solution of 4-amino-2-(methylthio)pyrimidine-5-carbonitrile (3.0 g, 18.05 mmol) in THF (100 mL) is added diisobutylaluminum hydride (41.52 mL, 1.0 M in CH2Cl2, 41.52 mmol) at 0° C. After the mixture is stirred for 2.5 hours at 0° C., hydrochloric acid (2N, 30 mL) is added and stirring is continued for 20 minutes. To the reaction mixture is added saturated Na2CO3 until a pH of 8 is achieved. The suspended material is filtered through Celit pad and washed with K2CO3 solution. The solution is diluted with EtOAc and washed with saturated K2CO3, brine and dried, filtered and concentrated to give crude product, which is purified by flash silica gel column, eluting with hexane (100%) gradient to hexane/ether (60/40%), to give the title intermediate as a solid (1.62 g, 53.1%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07449582B2
出典データセットuspto-grants-2008_11
ORD IDord-4f82a12b8b6b4e0b823e207cd72b0dda
出典メモuspto-grants-2008_11