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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 644209생성일: 2026년 10월 23일

2-amino-N-(5-chloropyridin-2-yl)benzamide → 2-[4-(B enzyloxy)-2-(1-tert-butoxycarbonylpiperidin-4-yloxy)benzoylamino]-N-(5-chloropyridin-2-yl)benzamide

https://huagongshe.com/ko/reaction/644209

반응식

참여 물질

역할이름HCID투입량
반응물2-amino-N-(5-chloropyridin-2-yl)benzamideHCID 21906381—
반응물4-Benzyloxy-2-(1-tert-butoxycarbonylpiperidin-4-yloxy)benzoic acidHCID 68535719—
생성물2-[4-(B enzyloxy)-2-(1-tert-butoxycarbonylpiperidin-4-yloxy)benzoylamino]-N-(5-chloropyridin-2-yl)benzamideHCID 68532666—

반응 단계

Using methods substantially equivalent to those described in Example 1-F, 4-benzyloxy-2-(1-tert-butoxycarbonylpiperidin-4-yloxy)benzoic acid (529 mg, 1.27 mmol) and N-(5-chloropyridin-2-yl)-2-aminobenzamide (297 mg, 1.20 mmol) afforded, after purification by chromatography (SiO2: EtOAc in hexanes), 493 mg (63%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07700628B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-b362c472deaa453eac5060bc7a1ee1e1
출처 메모uspto-grants-2010_04