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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 900300생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물3-(4-Aminophenyl)-1,3-dihydroquinazoline-2,4-dione trifluoroacetateHCID 22064391—
반응물(Tert-butyl)[(5-chloro-3-fluoro(2-thienyl))sulfonyl]amineHCID 22064462—
용매Trifluoroacetic acidHCID 6422—
생성물n-[4-(2,4-Dioxo(1,3-dihydroquinazolin-3-yl))phenyl]{[(5-chloro-3-fluoro(2-thienyl))sulfonyl]amino}carboxamideHCID 2206442634%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07358257B2
출처 데이터셋uspto-grants-2008_04
ORD IDord-1b1324261d86410bb5ab57a82d33a47a
출처 메모uspto-grants-2008_04