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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1174211생성일: 2026년 10월 25일

Triphenylphosphine → tert-butyl(2S,3S)-2-(2,4-dioxo-3-{[2-(3-pyridinyl)-1,3-thiazol-4-yl]methyl}-1-imidazolidinyl)-3-methylpentanoate

https://huagongshe.com/reaction/1174211

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물(2-Pyridin-3-yl-1,3-thiazol-4-yl)methanolHCID 4961264—
반응물tert-butyl(2S,3S)-2-(2,4-dioxo-1-imidazolidinyl)-3-methylpentanoateHCID 66891458—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물tert-butyl(2S,3S)-2-(2,4-dioxo-3-{[2-(3-pyridinyl)-1,3-thiazol-4-yl]methyl}-1-imidazolidinyl)-3-methylpentanoateHCID 67406421—

반응 조건

온도25 °C

반응 단계

A solution containing the product from Example 36C (0.081 g, 0.30 mmol) in dichloromethane (2 mL) at 0° C. was treated with the product from Example 57A (0.063 g, 0.33 mmol), triphenylphosphine (0.103 g, 0.39 mmol), followed by diethyl azodicarboxylate (0.061 mL, 0.39 mmol), stirred at 25° C. for 16 hours. Water (3 mL) was added and the reaction was stirred for 2 hours at 25° C. The reaction mixture was partitioned between dichloromethane and water, and the organic phase was washed with brine and dried over MgSO4, filtered and concentrated, to give the crude product, which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07834043B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-690d83dfd2294cdcbdd09e5a13bd933e
출처 메모uspto-grants-2010_11