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HRID 16872作成日:2026年10月26日

Diisopropylethylamine → Methyl 2-(3-(methoxymethyl)piperazin-1-yl)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/16872

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Methyl 2-chloropyrimidine-5-carboxylateHCID 12627752—
反応物2-(Methoxymethyl)piperazineHCID 14230264—
溶媒DichloromethaneHCID 6344—
生成物Methyl 2-(3-(methoxymethyl)piperazin-1-yl)pyrimidine-5-carboxylateHCID 6658994075%

反応手順

A solution of methyl 2-chloropyrimidine-5-carboxylate (300 mg, 1.74 mmol) in DCM (4.70 mL) was added to a stirred solution of 2-(methoxymethyl)piperazine (226 mg, 1.74 mmol) and N-ethyl-N-propan-2-ylpropan-2-amine (0.752 mL, 4.35 mmol) in DCM (4.00 mL) at 25° C. under nitrogen. The resulting solution was stirred at room temperature for 6 h. The reaction mixture was concentrated and diluted with MeOH. The resulting mixture was filtered. The filtrate was purified by ion exchange chromatography, using a SCX column. The desired product was eluted from the column using 7M NH3/MeOH and fractions were evaporated to dryness to afford methyl 2-(3-(methoxymethyl)piperazin-1-yl)pyrimidine-5-carboxylate (346 mg, 75%) as a yellow solid. This was used directly with no further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737149B2
出典データセットuspto-grants-2010_06
ORD IDord-80b8d9ce25f441588d5433e82862296a
出典メモuspto-grants-2010_06