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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 977081생성일: 2026년 10월 27일

Potassium Carbonate → 2-((2(RS)-(Phenoxymethyl)morpholin-4-yl)methyl)benzimidazole

https://huagongshe.com/reaction/977081

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-ChloromethylbenzimidazoleHCID 78571—
반응물2-(Phenoxymethyl)morpholineHCID 22011795—
용매EthanolHCID 702—
생성물2-((2(RS)-(Phenoxymethyl)morpholin-4-yl)methyl)benzimidazoleHCID 1996442066%

반응 단계

2-(Chloromethyl)benzimidazole (172 mg, 1.03 mmol) and 2(RS)-(phenoxymethyl)morpholine (200 mg) were heated in ethanol (8 ml) at 80° C. (oil bath temperature) in the presence of potassium carbonate (142 mg, 1.03 mmol) for 2 hours. The mixture was cooled then evaporated to dryness. The residue was partitioned between water (10 ml) and ethyl acetate (25 ml). The organic layer was separated and the aqueous re-extracted with ethyl acetate (25 ml). The combined organics were dried (sodium sulphate) then evaporated to give a beige gum which was purified by column chromatography on silica (150 g) using ethyl acetate to ethyl acetate/methanol (25:1) to afford the title compound as a pale yellow solid (220 mg, 66%). mp 171°-172° C. (ethyl acetate/n-hexane). MS, CI+, mz=324 for (M+H)+. 1H NMR (360 MHz, CDCl3) δ2.40 (1H, dd, J1 =J2 =10 Hz), 2.51 (1H, ddd, J1 =3, J2 =J3 =10 Hz), 2.79 (1H, d, J=10 Hz), 2.99 (1H, d, J=10 Hz), 3.82 (1H, ddd, J1 =3, J2 =J3 =10 Hz), 3.91-4.06 (6H, m), 6.88 (2H, dd, J1 =1, J2 =8 Hz), 6.95 (1H, ddd, J1 =1, J2 =J3 =8 Hz), 7.24-7.29 (4H, m), 7.57-7.61 (2H, m). Found: C, 70.55; H, 6.51; N, 12.96. C19H21N3O2 requires C, 70.57; H, 6.55; N, 12.99%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05614518
출처 데이터셋uspto-grants-1997_03
ORD IDord-a30d1054474d49b8973720ff13c3174a
출처 메모uspto-grants-1997_03