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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 61860생성일: 2026년 10월 23일

Triphenylphosphine → 7-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl methoxy)-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile

https://huagongshe.com/ko/reaction/61860

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참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물(R)-SolketalHCID 736056—
반응물7-methoxy-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrileHCID 66835270—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물7-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl methoxy)-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrileHCID 66834531—

반응 조건

온도50 °C

반응 단계

Under nitrogen atmosphere, 7-methoxy-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile (Compound W3, 15 mg, 0.05 mmol) and triphenylphosphine (40 mg, 3 eq.) were added with THF (1 ml), further added dropwise with ((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-methanol (20 mg, 3 eq.) and 2.19 N toluene solution of diethyl azodicarboxylate (68 μL, 3 eq.), and the mixture was stirred at 50° C. for 2 hr. After cooling, the reaction solution was added with ethyl acetate, washed with brine, dried over sodium sulfate, and filtered. The residues obtained after concentration under reduced pressure were purified by preparative TLC (ethyl acetate/dichloromethane), and the resulting solid was washed with dichloromethane to obtain the target compound (brown powder, 5 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440922B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-4b8e140ba2db4cb3834f3c390b3c7ae3
출처 메모uspto-grants-2016_09