돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 271640생성일: 2026년 10월 26일

Morpholine → 4-{4-[4-(5-Bromo-pyridin-2-yl)-but-3-ynyl]-benzyl}-morpholine

https://huagongshe.com/reaction/271640

반응식

참여 물질

역할이름HCID투입량
반응물MorpholineHCID 8083—
반응물Methanesulfonyl chlorideHCID 31297—
반응물DiisopropylethylamineHCID 81531—
반응물{4-[4-(5-Bromo-pyridin-2-yl)-but-3-ynyl]-phenyl}-methanolHCID 69070552—
용매DichloromethaneHCID 6344—
생성물4-{4-[4-(5-Bromo-pyridin-2-yl)-but-3-ynyl]-benzyl}-morpholineHCID 69079684—

반응 조건

온도0 °C

반응 단계

36 μL (0.46 mmol) methanesulphonic acid chloride are added to a solution, cooled to 0° C., of 120 mg (0.38 mmol) {4-[4-(5-bromo-pyridin-2-yl)-but-3-ynyl]-phenyl}-methanol (Example 2.20a) in 5 mL DCM. A solution of 78 μL (0.46 mmol) ethyldiisopropylamine in 1 mL DCM is slowly added dropwise, the mixture is stirred for a further 30 min at 0° C., then 80 μL (0.92 mmol) of morpholine are added, the mixture is allowed to come up to RT and kept at RT for 2 h. The mixture is evaporated down i.vac., the residue is combined with 20 mL EtOAc and 10 mL water, acidified with 1 M HCl and the phases are separated. The aqueous phase is combined with 2 M Na2CO3 solution, extracted with 20 mL EtOAc and the organic phase is dried over Na2SO4. After the desiccant and solvent have been eliminated the product is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07452911B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-c8f8424bdfa542bcad375fc370055782
출처 메모uspto-grants-2008_11