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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 493590생성일: 2026년 10월 25일

4,5-Diaminopyrimidine → 4-Amino-5-[(1-t-butoxycarbonylpiperidin-4-yl)amino)pyrimidine

https://huagongshe.com/reaction/493590

반응식

참여 물질

역할이름HCID투입량
반응물4,5-DiaminopyrimidineHCID 83703—
반응물tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매1,1-DichloroethaneHCID 6365—
생성물4-Amino-5-[(1-t-butoxycarbonylpiperidin-4-yl)amino)pyrimidineHCID 22293202—

반응 단계

A mixture of 4,5-diaminopyrimidine (1.0 g, 9.1 mmol), N-(t-butoxycarbonyl)-4-piperidone (3.0 g, 15 mmol) and sodium triacetoxyborohydride (1.2 g, 5.6 mmol) in dichloroethane (60 mL) was stirred at room temperature for 3 d. The reaction was partitioned between chloroform (200 mL) and 3N sodium hydroxide (30 mL). After drying over magnesium sulfate, the organic phase was concentrated to give the title compound as a tan gum. MS 294 (M+1)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07534784B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-9e97fb913b8e49cb9bacbe9a0c586c63
출처 메모uspto-grants-2009_05