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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 520440생성일: 2026년 10월 26일

Pyridine-3-sulfonyl chloride hydrochloride → N-(3-methyl-4-oxo-2-phenyl-3,4-dihydroquinazolin-8-yl)pyridine-3-sulfonamide

https://huagongshe.com/reaction/520440

반응식

참여 물질

역할이름HCID투입량
반응물Pyridine-3-sulfonyl chloride hydrochlorideHCID 12571517—
반응물8-amino-3-methyl-2-(3-(trifluoromethyl)phenyl)quinazolin-4(3H)-oneHCID 58552822—
용매PyridineHCID 1049—
생성물N-(3-methyl-4-oxo-2-phenyl-3,4-dihydroquinazolin-8-yl)pyridine-3-sulfonamideHCID 6799319462.7%

반응 조건

온도80 °C

반응 단계

Pyridine-3-sulfonyl chloride hydrochloride 7 (280 mg, 1.3 mmol) was added to a solution of 8-amino-3-methyl-2-(3-(trifluoromethyl)phenyl)quinazolin-4(3H)-one 5 (100 mg, 0.313 mmol) in pyridine (5 mL). The reaction mixture was heated at 80° C. for 12 h. The pyridine was removed in vacuo. The residue was taken up in CH2Cl2, washed with sat. aq NaHCO3, dried (MgSO4) and concentrated. The crude residue was purified by MPLC eluting with CH2Cl2/MeOH (0-10%) followed by recrystallization from CH3CN to give Compound 361 (77 mg, 53% yield). MS (ESI) calcd for C21H15F3N4O3S: 460.08. found: 461 [M+H].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09326986B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-4b14d276c9464054b64576a01ecda094
출처 메모uspto-grants-2016_05