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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 901085생성일: 2026년 10월 26일

Triphenylphosphine → morpholino(5-(3-(piperidin-1-yl)propoxy)-1H-indol-2-yl)methanone

https://huagongshe.com/reaction/901085

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Piperidine-1-propanolHCID 66032—
반응물(5-hydroxy-1H-indol-2-yl)-morpholin-4-yl-methanoneHCID 44185244—
용매TetrahydrofuranHCID 8028—
생성물morpholino(5-(3-(piperidin-1-yl)propoxy)-1H-indol-2-yl)methanoneHCID 11603156—

반응 단계

A mixture of 246 mg (1 mmol) (5-hydroxy-1H-indol-2-yl)-morpholin-4-yl-methanone, 1 g (ca. 3 mmol) polymerbound triphenylphospine (Fluka), 179 mg (1.25 mmol) piperidinepropanol and 461 mg (2 mmol) di-tert.-butyl azadicarboxylate in 20 ml THF was stirred for a prolonged period of time at room temperature. The mixture was filtered through a pad of silica and washed with 30 ml THF. The mixture was evaporated to dryness and purified on silica eluting with a gradient of DCM/2N NH3 in methanol 98/2 to DCM/2N NH3 in methanol 9/1. The product fractions were evaporated and the residue was titurated with diethyl ether to yield after drying at 40° C. under vacuum 47 mg (13%) of the title compound as white solid. MS (m/e): 372.4 (MH+, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07361682B2
출처 데이터셋uspto-grants-2008_04
ORD IDord-a469e94487064f219429eef4992a5248
출처 메모uspto-grants-2008_04