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HRID 29818作成日:2026年10月25日

Methylamine → 2-chloro-N-methyl-5-nitropyrimidin-4-amine

https://huagongshe.com/reaction/29818

反応式

関与物質

役割名称HCID仕込み量
反応物MethylamineHCID 6329—
反応物2,4-Dichloro-5-nitropyrimidineHCID 521266—
溶媒TetrahydrofuranHCID 8028—
生成物2-chloro-N-methyl-5-nitropyrimidin-4-amineHCID 714723299.3%

反応手順

A solution of 2,4-dichloro-5-nitropyrimidine (7.26 g, 37.4 mmol) in THF (100 ml) is cooled to −78° C. A solution of methyl amine (8 M in methanol, 9.35 mL, 74.8 mmol) is added dropwise. The mixture is allowed to warm to room temperature, and concentrated. The residue is partitioned between ethyl acetate and water. The layer is separated and the aqueous layer is extracted with ethyl acetate. The combined organic extracts are washed with brine, dried over Na2SO4, filtered and concentrated to afford the title product (7.0 g). (Note: the product contains 5% regio-isomer, 4-chloro-2-(methylamino)-5-nitropyrimidine). The residue is used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423038B2
出典データセットuspto-grants-2008_09
ORD IDord-83d91350d3d04fa4bc5182a219334930
出典メモuspto-grants-2008_09