돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 631598생성일: 2026년 10월 26일

Water → 1-(5-Tert-butylisoxazol-3-yl)-3-(5-(6,7-dimethoxyquinazolin-4-yloxy)-2,4-difluorophenyl)urea

https://huagongshe.com/reaction/631598

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물DiisopropylethylamineHCID 81531—
반응물Phenyl 5-tert-butylisoxazol-3-ylcarbamateHCID 13489605—
반응물5-(6,7-Dimethoxyquinazolin-4-yloxy)-2,4-difluoroanilineHCID 66876754—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매TetrahydrofuranHCID 8028—
생성물1-(5-Tert-butylisoxazol-3-yl)-3-(5-(6,7-dimethoxyquinazolin-4-yloxy)-2,4-difluorophenyl)ureaHCID 5666524825.1%

반응 조건

온도70 °C

반응 단계

To a solution of 5-(6,7-dimethoxyquinazolin-4-yloxy)-2,4-difluoroaniline (100 mg, 0.3 mmol) in THF (10 mL), DIEA (58 mg, 0.45 mmol), DMAP (20 mg, 0.16 mmol), and phenyl 5-tert-butylisoxazol-3-ylcarbamate (117 mg, 0.32 mmol) were added and the mixture heated overnight at 70° C. The mixture was poured into water and extracted with EtOAc three times. The extracts were dried over magnesium sulfate, filtered, and concentrated. The residue was purified using silica gel chromatography eluting with EtOAc/Hexane (3-80%). The appropriate fractions were concentrated to afford 1-(5-tert-butylisoxazol-3-yl)-3-(5-(6,7-dimethoxyquinazolin-4-yloxy)-2,4-difluorophenyl)urea (37.56 mg, 25% yield). 1H NMR (300 MHz, CDCl3) δ 1.35 (s, 9H), 4.05 (s, 6H), 6.09 (s, 1H), 6.85 (s, 1H), 7.28 (s, 1H), 7.35 (s, 1H), 8.28 (m, 1H), 8.70 (s, 1H), 9.50 (s, 1H). LC-MS (ESI) m/z 500 (M+H)+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09320739B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-236afe88de4a453f8b0ac5bbded6c4f1
출처 메모uspto-grants-2016_04