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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 539723생성일: 2026년 10월 24일

Diisopropylethylamine → (R)-benzyl 4-(2-fluoro-3-(3-(2-methylpyridin-4-yl)ureido)benzyl)-2-methylpiperazine-1-carboxylate

https://huagongshe.com/ko/reaction/539723

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물TriphosgeneHCID 94429—
반응물4-Amino-2-methylpyridineHCID 728670—
반응물(R)-benzyl 4-(3-amino-2-fluorobenzyl)-2-methylpiperazine-1-carboxylateHCID 58919233—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물(R)-benzyl 4-(2-fluoro-3-(3-(2-methylpyridin-4-yl)ureido)benzyl)-2-methylpiperazine-1-carboxylateHCID 5891923427%

반응 조건

온도0 °C

반응 단계

To a 0° C. solution of triphosgene (150 mg, 0.50 mmol, 0.35 equiv) in THF (15 mL) was slowly added via cannula a solution of (R)-benzyl 4-(3-amino-2-fluorobenzyl)-2-methylpiperazine-1-carboxylate (500 mg, 1.4 mmol, 1.0 equiv) and DIPEA (485 μL, 18.5 mmol, 2.0 equiv) in THF (15 mL) over approximately 15 minutes. The solution was stirred for an additional 20 min at 0° C., and 4-amino-2-methylpyridine was then added. After stirring at room temperature overnight, the reaction was diluted with EtOAc, washed with aq. satd. NaHCO3 and brine, dried over sodium sulfate, filtered and concentrated in vacuo. Purification by reverse phase preparative HPLC provided (R)-benzyl 4-(2-fluoro-3-(3-(2-methylpyridin-4-yl)ureido)benzyl)-2-methylpiperazine-1-carboxylate (180 mg, 27%). LCMS m/z (APCI)=492.3 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871768B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-cac495ea6a9a4abf83e48b825f74c5bc
출처 메모uspto-grants-2014_10