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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 395841생성일: 2026년 10월 24일

Thionyl Chloride → 2-[[4-(4-Pyridyl)benzoyl]amino]-N-(4-methoxyphenyl)benzamide Hydrochloride

https://huagongshe.com/ko/reaction/395841

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물2-amino-N-(4-methoxyphenyl)benzamideHCID 478820—
반응물4-(Pyridin-4-yl)benzoic acidHCID 1520811—
용매PyridineHCID 1049—
용매TolueneHCID 1140—
생성물2-[[4-(4-Pyridyl)benzoyl]amino]-N-(4-methoxyphenyl)benzamide HydrochlorideHCID 1817443530.7%

반응 단계

To a stirring suspension of 4-(4-pyridyl)benzoic acid (0.2 g, 1 mmol) in toluene (35 mL) was added thionyl chloride (0.55 mL, 7.5 mmol) and the mixture was heated to reflux. After 1 h the solution was cooled and added to a solution of 2-amino-N-(4-methoxyphenyl)benzamide (0.176 g, 0.73 mmol) in pyridine (2 mL) and toluene (5 mL). After stirring for 48 h, the solvent was removed in vacuo and the residue was partitioned between ethyl acetate and water. The organic phase was separated and washed with sat. NaHCO3, brine and dried (MgSO4), filtered and concentrated to give 103 mg of brown solid which was chromatographed by RPHPLC Method B. Upon standing, a sample of the title compound (14 mg, 4%) crystalized from one of the product containing fractions.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06605626B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-f64df43c3e664dbc9dab3e6aa122d8da
출처 메모uspto-grants-2003_08