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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 272855생성일: 2026년 10월 26일

Triphenylphosphine → Dimethyl-(4-{4-[2-(1-methylpyrrolidin-2-yl)ethoxy]phenyl}-tetrahydropyran-4-ylmethyl)amine

https://huagongshe.com/reaction/272855

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물1-Methyl-2-pyrrolidineethanolHCID 93363—
반응물Diisopropyl azodicarboxylateHCID 5363146—
반응물4-(4-Dimethylaminomethyl-tetrahydro-pyran-4-yl)-phenolHCID 23091621—
용매TetrahydrofuranHCID 8028—
용매Ethylacetate heptaneHCID 21899848—
생성물Dimethyl-(4-{4-[2-(1-methylpyrrolidin-2-yl)ethoxy]phenyl}-tetrahydropyran-4-ylmethyl)amineHCID 2309166827.2%

반응 단계

4-(4-Dimethylaminomethyl-tetrahydro-pyran-4-yl)-phenol (405 mg, 1.72 mmol), 2-(1-methyl-pyrrolidin-2-yl)-ethanol (178 mg, 1.38 mmol), PPh3 (451 mg, 1.72 mmol), THF (8 ml) and DIAD (348 mg, 1.72 mmol) were reacted together according to general procedure C. The crude product was subjected to chromatography on alumina eluting with ethyl acetate:heptane (50:50) to provide the title compound (130 mg, 27%) as a colourless oil. 1H NMR (400 MHz, CDCl3) δ7.21 (d, 2H), 6.87 (d, 2H), 4.09-3.95 (m, 2H), 3.75 (dt, 2H), 3.55 (td, 2H), 3.09 (m, 1H), 2.40 (s, 2H), 2.35 (s, 3H), 2.30-1.99 (m, 6H), 1.96 (s, 6H), 1.93-1.63 (m, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456164B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-c7111172352f4bf3bcd314fcdbde6536
출처 메모uspto-grants-2008_11