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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2354072생성일: 2026년 10월 25일

Sodium Iodide → (1-{2-[3-(2,6-Dimethyl-pyridin-4-yl)-ureido]-ethyl}-piperidin-4-yl)-methyl-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2354072

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Sodium BicarbonateHCID 516892—
반응물4-N-Boc-4-N-Methyl-aminopiperidineHCID 2756806—
반응물1-(2-Chloro-ethyl)-3-(2,6-dimethyl-pyridin-4-yl)-ureaHCID 58816567—
용매TetrahydrofuranHCID 8028—
생성물(1-{2-[3-(2,6-Dimethyl-pyridin-4-yl)-ureido]-ethyl}-piperidin-4-yl)-methyl-carbamic acid tert-butyl esterHCID 68690307—

반응 조건

온도50 °C

반응 단계

A suspension of methyl-piperidin-4-yl-carbamic acid tert-butyl ester (3.57 g, 16.7 mmol), NaHCO3 (6.7 g, 79 mmol), NaI (1.5 g, 10 mmol) and 1-(2-chloro-ethyl)-3-(2,6-dimethyl-pyridin-4-yl)-urea (Example D1, 2.14 g 9.4 mmol) in THF (30 mL) is stirred at 50° C. for 14 days. The mixture is quenched with Na2CO3 (50 mL) and extracted with CH2Cl2 (5×50 mL). The organic extracts are washed with sat. aq. Na2CO3 (30 mL), dried (Na2SO4), filtered and evaporated. The residue is purified by FC to provide the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07750161B2
출처 데이터셋uspto-grants-2010_07
ORD IDord-1b496d75bbb24013afbe7cf37c2bc6be
출처 메모uspto-grants-2010_07