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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2045725생성일: 2026년 10월 25일

Triphenylphosphine → 1-t-Butyl 2-methyl (2S,4R)-4-[(3-chloroquinoxalin-2-yl)oxy]pyrrolidine-1,2-dicarboxylate

https://huagongshe.com/reaction/2045725

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참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물3-chloro-1H-quinoxalin-2-oneHCID 302705—
반응물Diisopropyl azodicarboxylateHCID 5363146—
반응물N-Boc-cis-4-hydroxy-L-proline methyl esterHCID 10752873—
용매TetrahydrofuranHCID 8028—
생성물1-t-Butyl 2-methyl (2S,4R)-4-[(3-chloroquinoxalin-2-yl)oxy]pyrrolidine-1,2-dicarboxylateHCID 5809141977%

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온도20 °C

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A solution of 3-chloroquinoxalin-2-ol (1.44 g, 7.97 mmol) and 1-tert-butyl 2-methyl (2S,4S)-4-hydroxypyrrolidine-1,2-dicarboxylate (2.05 g, 8.37 mmol) in THF (190 ml) was cooled to 0° C., then treated with PPh3 (2.51 g, 9.57 mmol). DIAD (1.86 ml, 9.57 mmol) was added dropwise, and the mixture was stirred at 20° C. for 1 h. After evaporation of the volatiles, the residue was purified on silica gel (gradient elution, 0-70% EtOAc/petroleum ether) to afford the title compound (2.5 g, 77%). LCMS (ES+) m/z 408 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08591878B2
출처 데이터셋uspto-grants-2013_11
ORD IDord-c5e941b6d7d04d40a8ecb5e7030d2752
출처 메모uspto-grants-2013_11