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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1526468생성일: 2026년 10월 27일

Morpholine-4-carboximidamide Hydrobromide → HCID 178451771, 화합물

https://huagongshe.com/reaction/1526468

반응식

참여 물질

역할이름HCID투입량
반응물Morpholine-4-carboximidamide HydrobromideHCID 2806564—
반응물tert-Butyl 4-(3-ethoxy-3-oxopropanoyl)piperidine-1-carboxylateHCID 6618868—
반응물HCID 22171225HCID 22171225—
용매EthanolHCID 702—
생성물HCID 178451771HCID 17845177140.5%

반응 단계

Morpholine-4-carboxamidine hydrobromide (0.267 g) and 4-(2-ethoxycarbonylacetyl)-piperidine-1-carboxylic acid tert-butyl ester (0.38 g, 1.27 mmol) were stirred in ethanol (10 mL) and diazobicycloundecane (285 μl) was added. The reaction stirred for 18 hours at room temperature. The ethanol was removed under reduced pressure and water (25 mL) was added. The solution was acidified (to pH=4) with acetic acid. The product was extracted with dichloromethane (4×30 mL). The dichloromethane was removed and crude product was purified twice on silica gel (Combiflash), eluting with 10% methanol in dichloromethane to provide 4-(6-hydroxy-2-morpholin-4-ylpyrimidin-4-yl)-piperidine-1-carboxylic acid tert-butyl ester (0.15 g, 40.5% yield) as a white solid. 1H NMR (300 MHz, CDCl3/TMS): δ=5.63 (s, 1H), 4.25-4.05 (m, 2H), 3.75 (m, 8H), 2.75-2.65 (m, 2H), 2.47-2.35 (m, 1H), 1.00-1.75 (m, 2H), 1.70-1.50 (m, 2H), 1.46 (s, 9H). 13C NMR (75 MHz, CDCl3/TMS): δ=173.35, 166.87, 154.96, 154.06, 98.88, 79.70, 66.72, 45.13, 44.24, 30.64, 28.82, 27.58.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09085585B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-81446ba8b57b4be7832b57fa4a1caea4
출처 메모uspto-grants-2015_07