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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 403467생성일: 2026년 10월 25일

Cyclopentanol → [4-(5-Cyclopentyloxy-7-propoxy-oxazolo[5,4-d]pyrimidin-2-yl)-2,6-dimethyl-phenoxy]-acetic acid tert-butyl ester

https://huagongshe.com/reaction/403467

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참여 물질

역할이름HCID투입량
반응물CyclopentanolHCID 7298—
반응물tert-Butylimino-tri(pyrrolidino)phosphoraneHCID 3856267—
반응물Tert-butyl [4-(5-methanesulfonyl-7-propoxyoxazolo[5,4-d]pyrimidin-2-yl)-2,6-dimethylphenoxy]acetateHCID 86679896—
생성물[4-(5-Cyclopentyloxy-7-propoxy-oxazolo[5,4-d]pyrimidin-2-yl)-2,6-dimethyl-phenoxy]-acetic acid tert-butyl esterHCID 8667989827.2%

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온도100 °C

반응 단계

A solution of 98 mg of [4-(5-methanesulfonyl-7-propoxy-oxazolo[5,4-d]pyrimidin-2-yl)-2,6-dimethyl-phenoxy]-acetic acid tert-butyl ester, 19 mg of cyclopentanol and 69 mg of (tert-butylimino)tris(pyrrolidino)phosphorane was reacted at room temperature for 16 h and subsequently heated in a microwave reactor to 100° C. for 10 min. The mixture was poured onto water and extracted twice with ethyl acetate. The combined organic layers were washed with a 10% aqueous solution of citric acid and brine, dried and evaporated. After purification by preparative HPLC, 27 mg of the title compound were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08748436B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-31c921d7ce224a1fae567d02eb829044
출처 메모uspto-grants-2014_06