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HRID 1097729作成日:2026年10月27日

Morpholine → 8-Chloro-1-(5-{5-[(3,4-dichlorophenyl)methyl]-2H-tetrazol-2-yl}pentyl)-3-pentyl-3,7-dihydro-1H-purine-2,6-dione

https://huagongshe.com/reaction/1097729

反応式

関与物質

役割名称HCID仕込み量
反応物MorpholineHCID 8083—
反応物TriphenylphosphineHCID 11776—
反応物Dibenzyl azodicarboxylateHCID 5387121—
反応物7-Allyl-8-chloro-3-pentyl-1H-purine-2,6(3H,7H)-dioneHCID 59299557—
反応物5-{5-[(3,4-dichlorophenyl)methyl]-2H-tetrazol-2-yl}-1-pentanolHCID 66812959—
触媒HCID 178418397HCID 178418397—
溶媒TetrahydrofuranHCID 8028—
生成物8-Chloro-1-(5-{5-[(3,4-dichlorophenyl)methyl]-2H-tetrazol-2-yl}pentyl)-3-pentyl-3,7-dihydro-1H-purine-2,6-dioneHCID 59395605—

反応手順

To a solution of 8-chloro-3-pentyl-7-(2-propen-1-yl)-3,7-dihydro-1H-purine-2,6-dione (0.18 g, 0.61 mmol) in THF (5 ml) was added 5-{5-[(3,4-dichlorophenyl)methyl]-2H-tetrazol-2-yl}-1-pentanol (0.191 g, 0.61 mmol; prepared in similar fashion to Example 35), triphenylphosphine (0.36 g, 1.3 mmol) and finally dibenzylazodicarboxylate (0.40 g, 1.3 mmol). The solution was stirred for 18 h after which Pd(PPh3)4 (0.16 g, 0.137 mmol) followed by morpholine (0.75 ml, 8.3 mmol) was added and the solution stirred at ambient temperature for 6 h. The solution was loaded onto an aminopropyl SPE (5 g) and eluted with MeOH then 5% AcOH/MeOH to yield the title compound containing minor impurities. Further chromatography (silica SPE, 20 g) eluting with ether yielded the title compound as a white solid (0.061 g, 18%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08143264B2
出典データセットuspto-grants-2012_03
ORD IDord-4a068786fca049eea1de852f28f58bca
出典メモuspto-grants-2012_03