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HRID 520440作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物Pyridine-3-sulfonyl chloride hydrochlorideHCID 12571517—
反応物8-amino-3-methyl-2-(3-(trifluoromethyl)phenyl)quinazolin-4(3H)-oneHCID 58552822—
溶媒PyridineHCID 1049—
生成物N-(3-methyl-4-oxo-2-phenyl-3,4-dihydroquinazolin-8-yl)pyridine-3-sulfonamideHCID 6799319462.7%

反応条件

温度80 °C

反応手順

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].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09326986B2
出典データセットuspto-grants-2016_05
ORD IDord-4b14d276c9464054b64576a01ecda094
出典メモuspto-grants-2016_05