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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2200908생성일: 2026년 10월 24일

Methanol → 4-[(3-Chloro-4-methoxybenzyl)amino]-2-[(2S)-2-(hydroxymethyl)-pyrrolidin-1-yl]pyrimidine-5-carboxylic acid

https://huagongshe.com/ko/reaction/2200908

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Ethyl 4-((3-chloro-4-methoxy-phenyl)methylamino)-2-((2S)-2-(hydroxymethyl)pyrrolidin-1-yl)pyrimidine-5-carboxylateHCID 52348789—
반응물Sodium monohydrateHCID 71353970—
용매WaterHCID 962—
생성물4-[(3-Chloro-4-methoxybenzyl)amino]-2-[(2S)-2-(hydroxymethyl)-pyrrolidin-1-yl]pyrimidine-5-carboxylic acidHCID 6711933548.1%

반응 단계

Methanol (50 mL) was added in ethyl (s)-4-((3-chloro-4-methoxybenzyl)amino)-2-(2-(hydroxymethyl)tetrahydropyrrole-1-yl)-5-pyrimidine carboxylate (8.75 g, 20.8 mmol). In water (20 mL) was dissolved sodium hydrate (1.66 g, 41.6 mmol), then the aqueous solution was added to the reaction solution. The reaction was conducted in an oil bath of 50 to 60° C. overnight. The reaction was monitored by LC-MS. The organic solvent was removed by rotary evaporation. The residual aqueous phase was adjusted to a pH of 3 to 4. Then solid was precipitated. The precipitation was filtrated and dried to give a solid (3.9 g, 48.1% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09359371B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-caed84a4441748fb83a08326067543fe
출처 메모uspto-grants-2016_06