돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1790682생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1790682

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 번호US07071216B2
출처 데이터셋uspto-grants-2006_07
ORD IDord-0a79efa2b0854b679e5635cea251931d
출처 메모uspto-grants-2006_07