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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 922954생성일: 2026년 10월 27일

4-(((tert-Butoxycarbonyl)amino)methyl)benzoic acid → Tert-butyl 4-(4-chloro-3-(pyridin-2-yl)phenylcarbamoyl)benzylcarbamate

https://huagongshe.com/reaction/922954

반응식

참여 물질

역할이름HCID투입량
반응물4-(((tert-Butoxycarbonyl)amino)methyl)benzoic acidHCID 853605—
반응물4-Chloro-3-(pyridin-2-yl)anilineHCID 40151925—
생성물Tert-butyl 4-(4-chloro-3-(pyridin-2-yl)phenylcarbamoyl)benzylcarbamateHCID 66878147—

반응 단계

75 mg of 4-chloro-3-(pyridin-2-yl)aniline was coupled to 4-((tert-butoxycarbonylamino)methyl)benzoic acid via Procedure G to yield tert-butyl 4-(4-chloro-3-(pyridin-2-yl)phenylcarbamoyl)benzylcarbamate. Tert-butyl 4-(4-chloro-3-(pyridin-2-yl)phenylcarbamoyl)benzylcarbamate was subsequently treated with 4N HCl in Dioxane to remove the Boc protecting group and form the HCl salt of 4-(aminomethyl)-N-(4-chloro-3-(pyridin-2-yl)phenyl)benzamide. 50 mg of the crude HCl salt of 4-(aminomethyl)-N-(4-chloro-3-(pyridin-2-yl)phenyl)benzamide was coupled to picolinic acid via Procedure G. The crude product was purified by reverse phase HPLC to yield N-(4-(4-chloro-3-(pyridin-2-yl)phenylcarbamoyl)benzyl)picolinamide. MS (Q1) 443.3 (M)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09278961B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-ee2b56f91bcc47308f9e104cef1c7be3
출처 메모uspto-grants-2016_03