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HRID 3169作成日:2026年10月24日

Ethyl 4-(methylamino)-2-(methylsulfanyl)pyrimidine-5-carboxylate → (4-(Methylamino)-2-(methylthio)pyrimidin-5-yl)methanol

https://huagongshe.com/ja/reaction/3169

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 4-(methylamino)-2-(methylsulfanyl)pyrimidine-5-carboxylateHCID 295697—
反応物Aluminium lithium hydrideHCID 21226445—
溶媒TetrahydrofuranHCID 8028—
生成物(4-(Methylamino)-2-(methylthio)pyrimidin-5-yl)methanolHCID 1067909284%

反応手順

A solution of 4-methylamino-2-methylsulfanyl-5-pyrimidinecarboxylate ethyl ester (4.36 g, 19.3 mmol) in 60 mL of tetrahydrofuran was added dropwise to a room temperature suspension of lithium aluminum hydride (1.10 g, 29.0 mmol) in 40 mL of tetrahydrofuran. After 10 minutes the reaction was carefully quenched with 2 mL of water, 2 mL of 15% NaOH, and an additional 7 mL of water. The mixture was stirred for 1 hour, and the white precipitate which had formed was removed by filtration, and was washed with ethyl acetate. The filtrate was concentrated in vacuo and 3:1 hexane:ethyl acetate was added. The solids were collected to give 2.99 g (84%) of 4-methylamino-2-methylsulfanyl-5-pyrimidinemethanol; mp 155°-157° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05733914
出典データセットuspto-grants-1998_03
ORD IDord-abfc9b5568f94a61bc5a0e552cd345d3
出典メモuspto-grants-1998_03