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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2212346생성일: 2026년 10월 26일

3-Pyridinecarbonyl chloride, hydrochloride (1:1) → N-[4-(4-Methoxyphenyl)-5-{2-[(pyridine-3-carbonyl)amino]pyridin-4-yl}-1,3-thiazol-2-yl]pyridine-3-carboxamide

https://huagongshe.com/reaction/2212346

반응식

참여 물질

역할이름HCID투입량
반응물3-Pyridinecarbonyl chloride, hydrochloride (1:1)HCID 88438—
반응물Sodium BicarbonateHCID 516892—
반응물4-[2-Amino-4-(4-methoxyphenyl)-1,3-thiazol-5-yl]-2-pyridylamineHCID 9966038—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DimethylacetamideHCID 31374—
생성물N-[4-(4-Methoxyphenyl)-5-{2-[(pyridine-3-carbonyl)amino]pyridin-4-yl}-1,3-thiazol-2-yl]pyridine-3-carboxamideHCID 987090533%

반응 조건

온도70 °C

반응 단계

Nicotinoyl chloride hydrochloride (0.72 g, 4.1 mmol) and 4-dimethylaminopyridine (0.05 g, 0.4 mmol) were added to a solution of 4-[2-amino-4-(4-methoxyphenyl)-1,3-thiazol-5-yl]-2-pyridylamine (0.41 g, 1.4 mmol) in N,N-dimethylacetamide (10 mL) and the mixture was stirred at 70° C. for 19 hours. After the reaction mixture was cooled to room temperature, a saturated aqueous solution of sodium hydrogencarbonate (50 mL) was added. The resulting crude crystals were collected by filtration and washed with water. The crude crystals were recrystallized from ethanol to obtain 0.23 g (0.44 mmol, yield 33%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07101899B1
출처 데이터셋uspto-grants-2006_09
ORD IDord-97c70ef57e1046a68df529d66d38fed8
출처 메모uspto-grants-2006_09