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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29818생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/29818

반응식

참여 물질

역할이름HCID투입량
반응물MethylamineHCID 6329—
반응물2,4-Dichloro-5-nitropyrimidineHCID 521266—
용매TetrahydrofuranHCID 8028—
생성물2-chloro-N-methyl-5-nitropyrimidin-4-amineHCID 714723299.3%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423038B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-83d91350d3d04fa4bc5182a219334930
출처 메모uspto-grants-2008_09