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HRID 901085作成日:2026年10月26日

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

https://huagongshe.com/reaction/901085

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Piperidine-1-propanolHCID 66032—
反応物(5-hydroxy-1H-indol-2-yl)-morpholin-4-yl-methanoneHCID 44185244—
溶媒TetrahydrofuranHCID 8028—
生成物morpholino(5-(3-(piperidin-1-yl)propoxy)-1H-indol-2-yl)methanoneHCID 11603156—

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07361682B2
出典データセットuspto-grants-2008_04
ORD IDord-a469e94487064f219429eef4992a5248
出典メモuspto-grants-2008_04