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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 272870생성일: 2026년 10월 26일

(2R)-2-(Methoxymethyl)pyrrolidine → (R)-2-Methoxymethyl-1-{4-[4-(3-pyrrolidin-1-yl-propoxy)-phenyl]-tetrahydro-pyran-4-ylmethyl}-pyrrolidine

https://huagongshe.com/reaction/272870

반응식

참여 물질

역할이름HCID투입량
반응물(2R)-2-(Methoxymethyl)pyrrolidineHCID 671216—
반응물4-[4-(3-pyrrolidin-1-ylpropoxy)phenyl]tetrahydro-2H-pyran-4-carbaldehydeHCID 59837427—
촉매Titanium isopropoxideHCID 11026—
용매EthanolHCID 702—
생성물(R)-2-Methoxymethyl-1-{4-[4-(3-pyrrolidin-1-yl-propoxy)-phenyl]-tetrahydro-pyran-4-ylmethyl}-pyrrolidineHCID 1161141159.4%

반응 단계

4-[4-(3-Pyrrolidin-1-ylpropoxy)phenyl]tetrahydro-2H-pyran-4-carbaldehyde (500 mg, 1.575 mmol), (R)-2-(methoxymethyl)pyrrolidine (347 mg, 4.21 mmol), absolute ethanol (20 ml), activated 3 Å molecular sieves (500 mg), titanium (IV) isopropoxide (2.33 ml, 7.88 mmol) and STAB (2.84 g, 13.4 mmol) were reacted in accordance with the general procedure D. The isolated waxy solid was purified by column chromatography on silica eluting with DCM:MeOH:NH3 95:14:1 to give the title compound as a viscous pale yellow oil (390 mg, 59%). 1H NMR (400 MHz, CDCl3) δ7.18 (d, 2H), 6.86 (d, 2H), 4.02 (t, 2H), 3.85-3.69 (m, 2H), 3.59 (td, 1H), 3.45 (td, 1H), 3.27 (s, 3H), 3.10 (dd, 1H), 3.02 (dd, 1H), 2.94 (d, 1H), 2.63 (t, 2H), 2.58-2.45 (m, 6H), 2.39 (m, 1H), 2.21 (m, 1H), 2.07-1.67 (m, 11H), 1.57-1.33 (m, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456164B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-3db96ad8a53f460e91014ce84ac42750
출처 메모uspto-grants-2008_11