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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 539715생성일: 2026년 10월 24일

Diisopropylethylamine → Tert-butyl 4-(2-fluoro-3-(3-(2-methylpyridin-4-yl)ureido)benzyl)piperazine-1-carboxylate

https://huagongshe.com/ko/reaction/539715

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물TriphosgeneHCID 94429—
반응물4-Amino-2-methylpyridineHCID 728670—
반응물Tert-butyl 4-(3-amino-2-fluorobenzyl)piperazine-1-carboxylateHCID 58919232—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물Tert-butyl 4-(2-fluoro-3-(3-(2-methylpyridin-4-yl)ureido)benzyl)piperazine-1-carboxylateHCID 5891922643%

반응 조건

온도0 °C

반응 단계

To a 0° C. solution of triphosgene (959 mg, 3.24 mmol, 0.35 equiv) in THF (45 mL) was slowly added via cannula a solution of tert-butyl 4-(3-amino-2-fluorobenzyl)piperazine-1-carboxylate (2.86 g, 9.25 mmol, 1.0 equiv) and DIPEA (3.2 mL, 18.5 mmol, 2.0 equiv) in THF (25 mL) over approximately 20 minutes. The solution was stirred for an additional 15 min at 0° C., and 4-amino-2-methylpyridine was then added. After stirring at room temperature for 72 h, 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 tert-butyl 4-(2-fluoro-3-(3-(2-methylpyridin-4-yl)ureido)benzyl)piperazine-1-carboxylate (1.77 g, 43%). LCMS m/z (APCI)=444.3 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871768B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-d2596ea1680648daab9a84ecb290a8dc
출처 메모uspto-grants-2014_10