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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25207생성일: 2026년 10월 24일

N-(3-Aminopropyl)morpholine → 3-({1-[bis(4-chlorophenyl)methyl]azetidin-3-ylidene} methanesulfonylmethyl)-N-(3-morpholin-4-ylpropyl)benzamide

https://huagongshe.com/ko/reaction/25207

반응식

참여 물질

역할이름HCID투입량
반응물N-(3-Aminopropyl)morpholineHCID 61055—
반응물3-({1-[Bis(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)benzoic acidHCID 69635678—
용매DichloromethaneHCID 6344—
생성물3-({1-[bis(4-chlorophenyl)methyl]azetidin-3-ylidene} methanesulfonylmethyl)-N-(3-morpholin-4-ylpropyl)benzamideHCID 69635653—

반응 단계

0.0388 cm3 of N-(3-aminopropyl)morpholine is added, at the same temperature, to a suspension of 150 mg of 3-({1-[bis(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)benzoic acid activated on TFP resin (165 μM) in 3 cm3 of dichloromethane, pre-stirred for 90 minutes at a temperature close to 20° C. The suspension is stirred at a temperature close to 20° C. for 22 hours and then filtered on sintered glass. The solid residue is rewashed with twice 1.5 cm3 of dichloromethane. The filtrates are combined and concentrated to dryness under reduced pressure (2.7 kPa) at a temperature close to 40° C. 60 mg of 3-({1-[bis(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)-N-(3-morpholin-4-ylpropyl)benzamide are thus obtained in the form of a pale yellow foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858603B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-4634c880f5ca4716bd33fcdc4904024b
출처 메모uspto-grants-2005_02