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HRID 900300作成日:2026年10月26日

Acetonitrile → n-[4-(2,4-Dioxo(1,3-dihydroquinazolin-3-yl))phenyl]{[(5-chloro-3-fluoro(2-thienyl))sulfonyl]amino}carboxamide

https://huagongshe.com/reaction/900300

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物3-(4-Aminophenyl)-1,3-dihydroquinazoline-2,4-dione trifluoroacetateHCID 22064391—
反応物(Tert-butyl)[(5-chloro-3-fluoro(2-thienyl))sulfonyl]amineHCID 22064462—
溶媒Trifluoroacetic acidHCID 6422—
生成物n-[4-(2,4-Dioxo(1,3-dihydroquinazolin-3-yl))phenyl]{[(5-chloro-3-fluoro(2-thienyl))sulfonyl]amino}carboxamideHCID 2206442634%

反応手順

A 19 mg-sample (0.07 mmol) of (tert-butyl)[(5-chloro-3-fluoro(2-thienyl))sulfonyl]amine was dissolved in neat TFA and stirred for 1 h, concentrated in vacuo and used directly in the next transformation. This sample was dissolved in 150 uL of DCM and 21 mg (0.084 mmol) of DSC was added followed by 21 μL (0.14 mmol) of DBU. This solution was stirred for 18 h, 26 mg (0.07) of 3-(4-aminophenyl)-1,3-dihydroquinazoline-2,4-dione trifluoroacetate salt was added plus 150 μL of dry acetonitrile and refluxed for 2 h. This material was then purified on RP-HPLC to afford 11 mg (34%) of the desired product. ES-MS: M+H+=495 (Cl).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07358257B2
出典データセットuspto-grants-2008_04
ORD IDord-1b1324261d86410bb5ab57a82d33a47a
出典メモuspto-grants-2008_04