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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1887842생성일: 2026년 10월 25일

Triethylamine → 7-Chloro-3-{[(6-morpholin-4-yl-pyridine-3-carbonyl)-amino]-methyl}-4-oxo-1-phenyl-1,4-dihydro-quinoline-2-carboxylic acid dimethylamide

https://huagongshe.com/reaction/1887842

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물PyBroPHCID 2733179—
반응물6-Morpholinonicotinic AcidHCID 2776460—
반응물3-(aminomethyl)-7-chloro-N,N-dimethyl-4-oxo-1-phenyl-1,4-dihydroquinoline-2-carboxamideHCID 71208675—
용매DimethylformamideHCID 6228—
생성물7-Chloro-3-{[(6-morpholin-4-yl-pyridine-3-carbonyl)-amino]-methyl}-4-oxo-1-phenyl-1,4-dihydro-quinoline-2-carboxylic acid dimethylamideHCID 71208173—

반응 단계

6-Morpholinonicotinic acid (32.6 mg, 0.142 mmol), bromo-tris-pyrrolidino-phosphonium hexafluorophosphate (PyBrOP) (120 mg, 0.374 mmol) and triethylamine (100 mg, 0.137 mL, 0.988 mmol) were combined with DMF (4 mL). The reaction mixture was stirred at room temperature for 10 min. After this time, 3-(aminomethyl)-7-chloro-N,N-dimethyl-4-oxo-1-phenyl-1,4-dihydroquinoline-2-carboxamide (intermediate C) (0.052 g, 0.156 mmol) was added. The reaction mixture was stirred at room temperature for 15 hr. The crude material was purified by flash chromatography (10% ethyl acetate-hexanes ramped to 100% ethyl acetate). MS calcd. for C29H28ClN5O4 [(M+H)+] 546.2, obsd. 546.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08501732B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-daf8e8c7d2854c769e78497cb220f24f
출처 메모uspto-grants-2013_08