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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 408693생성일: 2026년 10월 24일

Sodium hydride → 5-chloro-1-(2-methoxy-ethoxymethyl)-6-pyrrolidin-1-yl-1H-benzoimidazole

https://huagongshe.com/ko/reaction/408693

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
반응물6-chloro-5-pyrrolidin-1-yl-1H-benzoimidazoleHCID 66937434—
용매TetrahydrofuranHCID 8028—
생성물5-chloro-1-(2-methoxy-ethoxymethyl)-6-pyrrolidin-1-yl-1H-benzoimidazoleHCID 66937238—

반응 조건

온도0 °C

반응 단계

To a mixture of 6-chloro-5-pyrrolidin-1-yl-1H-benzoimidazole (0.443 g, 2.00 mmol) and THF (5 mL) was added NaH (96.0 mg, 60% dispersion in mineral oil, 2.40 mmol) at 0° C. After stirring the reaction mixture for 30 min at 0° C., 1-chloromethoxy-2-methoxy-ethane (0.299 g, 2.40 mmol) was added and the mixture was stirred for 18 h. The reaction mixture was quenched with water and the aqueous layer was extracted with EtOAc (3×50 mL). The combined organic layers were washed with brine (2×20 mL), dried, filtered, and concentrated under reduced pressure. The residue was purified (FCC) (0-10% MeOH/DCM) to yield the titled compound as a mixture of regioisomers (0.240 g, 39%) with a purity of 90%. MS (ESI/CI): mass calcd. for C15H20ClN3O2, 309.1; m/z found, 310.1 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08759345B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-e81f870bd54b451985dc101c3ea04261
출처 메모uspto-grants-2014_06