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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13473생성일: 2026년 10월 25일

4-(Chloromethyl)benzoyl chloride → [4-(2-{[4-(Chloromethyl)phenyl]carbonylamino}-1-methylbenzimidazol-5-yloxy)(2-pyridyl)]-n-methylcarboxamide

https://huagongshe.com/reaction/13473

반응식

참여 물질

역할이름HCID투입량
반응물4-(Chloromethyl)benzoyl chlorideHCID 70136—
반응물Sodium thiocyanateHCID 516871—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물4-(3-Amino-4-methylamino-phenoxy)-pyridine-2-carboxylic acid methylamideHCID 17755838—
용매AcetoneHCID 180—
생성물[4-(2-{[4-(Chloromethyl)phenyl]carbonylamino}-1-methylbenzimidazol-5-yloxy)(2-pyridyl)]-n-methylcarboxamideHCID 131725840—

반응 단계

A solution of sodium thiocyanate (1 eq) in acetone was added slowly in to a solution of 4-(chloromethyl)benzoylchloride (1 eq) in acetone at 0° C. The mixture was then filtered in to a solution of {4-[3-amino-4-(methylamino)phenoxy](2-pyridyl)}-N-methylcarboxamide (1 eq) in acetone. Formation of N-acylthiourea was followed by LC/MS. The mixture was concentrated and taken in tetrahydrofuran and to it was added 1-ethyl-(3-dimethylaminopropyl)carbodimidehydrochloride (2 eq) and stirred at ambient temperature for 16 h. The mixture was concentrated and partitioned between ethyl acetate and water. The organic layer was then dried and concentrated to yield [4-(2-{[4-(chloromethyl)phenyl]carbonylamino)-1-methylbenzimidazol-5-yloxy)(2-pyridyl)]-N-methylcarboxamide. MS: MH+=449.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728010B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-145a31cfa28b4bfab5a9bc7ac5183ed4
출처 메모uspto-grants-2010_06