돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38169생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/38169

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. BS-MS: M+H+=495 (Cl).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524721B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-c402dd8d3437460b920d5e0d79eff05a
출처 메모uspto-grants-2013_09