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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1782710생성일: 2026년 10월 26일

Dichloromethane → 4-[2-(acetylamino)phenyl]-1,3-dihydro-1-[1-(phenylmethyl)-4-piperidinyl]-2H-benzimidazol-2-one

https://huagongshe.com/reaction/1782710

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물DiisopropylethylamineHCID 81531—
반응물1-Benzyl-4-piperidylamineHCID 415852—
반응물Sodium CyanateHCID 517096—
반응물N-[2-(2-bromoacetyl)phenyl]acetamideHCID 2749459—
용매Acetic AcidHCID 176—
용매Ethylacetate methanolHCID 21584119—
생성물4-[2-(acetylamino)phenyl]-1,3-dihydro-1-[1-(phenylmethyl)-4-piperidinyl]-2H-benzimidazol-2-oneHCID 18321183—

반응 단계

To a solution of 26.3 g (0.138 mol) of 4-amino-1-(phenylmethyl)piperidine and 17.8 g (0.138 mol) of DIEA in 300 ml of dichloromethane was added dropwise a solution of 35.4 g (0.138 mol) of 1-[2-(acetylamino)phenyl]-2-bromoethanone in 150 ml of dichloromethane and the mixture was kept for a further 2 hours at room temperature. With external cooling with ice 13.5 g (0.20 mol) of sodium cyanate and 12 ml of glacial acetic acid were then added and the mixture was stirred overnight in a thawing ice bath. It was washed with water and saturated sodium hydrogen carbonate solution, dried over sodium sulphate and freed from solvent. The residue was triturated with 50 ml of ethyl acetate-methanol mixture (9/1 v/v), the resulting crystals were suction filtered, washed with ethyl acetate and dried in vacuo. 37.0 g (68.7% of theory) of colourless crystals were obtained, Rf=0.41 (eluant: dichloromethane/methanol 9/1 v/v).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07498325B2
출처 데이터셋uspto-grants-2009_03
ORD IDord-0c9ef28bfebc44cb821975586637595e
출처 메모uspto-grants-2009_03