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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyridine-3-sulfonyl chloride hydrochloride | HCID 12571517 | — |
| 반응물 | 8-amino-3-methyl-2-(3-(trifluoromethyl)phenyl)quinazolin-4(3H)-one | HCID 58552822 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | N-(3-methyl-4-oxo-2-phenyl-3,4-dihydroquinazolin-8-yl)pyridine-3-sulfonamide | HCID 67993194 | 62.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09326986B2 |
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| 출처 데이터셋 | uspto-grants-2016_05 |
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| ORD ID | ord-4b14d276c9464054b64576a01ecda094 |
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| 출처 메모 | uspto-grants-2016_05 |
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