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HRID 1177633作成日:2026年10月27日

Triethylamine → N-(3-fluoro-4-(5-(1-phenylcyclopropyl)[1,3]thiazolo[5,4-b]pyridin-2-yl)phenyl)-N-(methylsulfonyl)methanesulfonamide

https://huagongshe.com/reaction/1177633

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methanesulfonyl chlorideHCID 31297—
反応物3-Fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)benzenamineHCID 57403052—
溶媒DichloromethaneHCID 6344—
生成物N-(3-fluoro-4-(5-(1-phenylcyclopropyl)[1,3]thiazolo[5,4-b]pyridin-2-yl)phenyl)-N-(methylsulfonyl)methanesulfonamideHCID 59174861—

反応手順

To 3-fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)benzenamine (34 mg, 0.094 mmol) was added DCM (0.9 mL), triethylamine (26 μl, 0.188 mmol), and methanesulfonyl chloride (11 μl, 0.141 mmol) before it was stirred at ambient T for 1 h. The reaction mixture was diluted with 100 mL of DCM, added to a separatory funnel, partitioned with 5 N NaOH (aqueous), washed 3 times with 75 mL of 5 N NaOH (aqueous), separated, dried over sodium sulfate, and concentrated via rotovap to the title compound. MS (ESI) m/z: Calculated: 517.1; Observed: 518.0 (M++1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07842685B2
出典データセットuspto-grants-2010_11
ORD IDord-6556fd319c5c4ef0be911c220784da14
出典メモuspto-grants-2010_11