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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40514생성일: 2026년 10월 24일

1,4-Dioxane → (S)-1-(1-{4-[3-(4-Ethoxy-phenoxy)-azetidin-1-yl]-phenyl}-ethyl)-3-pyrimidin-4-yl-urea

https://huagongshe.com/ko/reaction/40514

반응식

참여 물질

역할이름HCID투입량
반응물1,4-DioxaneHCID 31275—
반응물4-AminopyrimidineHCID 68958—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물(S)-1-{4-[3-(4-Ethoxy-phenoxy)-azetidin-1-yl]-phenyl}-ethylamineHCID 86689010—
생성물(S)-1-(1-{4-[3-(4-Ethoxy-phenoxy)-azetidin-1-yl]-phenyl}-ethyl)-3-pyrimidin-4-yl-ureaHCID 71616306—

반응 단계

0.03 mL (0.20 mmol) DBU and 0.033 g (0.20 mmol) CDT are added to 0.010 g (0.10 mmol) 4-aminopyrimidine in 1.0 mL 1,4-dioxane. The mixture is stirred for 5 min at rt followed by addition of 0.048 g (0.092 mmol) (S)-1-{4-[3-(4-ethoxy-phenoxy)-azetidin-1-yl]-phenyl}-ethylamine (X.1) in 1.0 mL 1,4-dioxane. The mixture is stirred for 12 h at rt and subsequently concentrated in vacuo. The residue is purified by HPLC (XBridge, ACN/water (+0.1% NH4OH)) to yield the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530461B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-30a23b06abe14314b3991ac4d9ca0352
출처 메모uspto-grants-2013_09