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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 61602생성일: 2026년 10월 24일

3-Butyn-2-amine, 2-methyl- → 2-(3-(4-(1H-indazol-5-ylamino)quinazolin-2-yl)phenoxy)-N-(2-methylbut-3-yn-2-yl)acetamide

https://huagongshe.com/ko/reaction/61602

반응식

참여 물질

역할이름HCID투입량
반응물3-Butyn-2-amine, 2-methyl-HCID 76319—
반응물DiisopropylethylamineHCID 81531—
반응물PyBOPHCID 2724699—
반응물2-(3-(4-((1H-indazol-5-yl)amino)quinazolin-2-yl)phenoxy)acetic acidHCID 59361988—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물2-(3-(4-(1H-indazol-5-ylamino)quinazolin-2-yl)phenoxy)-N-(2-methylbut-3-yn-2-yl)acetamideHCID 59361964—

반응 단계

A suspension of 2-(3-(4-(1H-indazol-5-ylamino)quinazolin-2-yl)phenoxy)acetic acid (70 mg, 0.14 mmol), PyBOP® (40 mg, 0.077 mmol), DIEA (24 μL, 0.14 mmol) in dry CH2Cl2:DMF (2:0.1 mL) was stirred at RT for 15 minutes. To this solution of activated acid was added 2-methylbut-3-yn-2-amine (7.6 mg, 0.091 mmol). After 30 minutes, 1.0 equivalent of DIEA and 0.55 equivalents of PyBOP® were added. After stirring the solution for 15 minutes, 0.65 equivalents of 2-methylbut-3-yn-2-amine were added and the mixture was stirred for an additional 30 minutes. The solvent was removed in vacuo and the crude product was purified using prep HPLC (20-45_90 mins) to afford 2-(3-(4-(1H-indazol-5-ylamino)quinazolin-2-yl)phenoxy)-N-(2-methylbut-3-yn-2-yl)acetamide. (22 mg, 0.046 mmol, 33%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440961B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-36d4d8a0eefe4455a4d28f38aca23464
출처 메모uspto-grants-2016_09