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HRID 525048作成日:2026年10月26日

Toluene → tert-butyl 9-(2-(3-chloro-2-(pyridin-4-ylcarbamoyl)-1H-pyrrol-1-ylamino)-2-oxoethyl)-9H-purin-6-ylcarbamate

https://huagongshe.com/reaction/525048

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物4-AminopyridineHCID 1727—
反応物Sodium tartrate-2-hydrateHCID 517351—
反応物TrimethylaluminumHCID 16682925—
反応物di-tert-butyl 9-((5-chloro-4-oxo-4H-pyrrolo[1,2-d][1,3,4]oxadiazin-2-yl)methyl)-9H-purin-6-ylimidodicarbonateHCID 70922312—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物tert-butyl 9-(2-(3-chloro-2-(pyridin-4-ylcarbamoyl)-1H-pyrrol-1-ylamino)-2-oxoethyl)-9H-purin-6-ylcarbamateHCID 7092226893.6%

反応手順

To a suspension of 4-aminopyridine (164 mg, 1.74 mmol) in 3.3 mL of dichloromethane under inert atmosphere was added a 2M solution of trimethyl aluminium in toluene (0.87 mL, 1.74 mmol) and the mixture was stirred during 20 minutes at room temperature. Next, this mixture was cooled in an ice-water bath and a solution of di-tert-butyl 9-((5-chloro-4-oxo-4H-pyrrolo[1,2-d][1,3,4]oxadiazin-2-yl)methyl)-9H-purin-6-ylimidodicarbonate (150 mg, 0.29 mmol) in 2.2 mL of dry dichloromethane was added stirring the mixture during 3 days at room temperature. At the end of this period, the reaction mixture was cooled-down with an ice-water bath and mL of water were added followed by a 5% aqueous solution disodium tartrate dihydrate. The resulting mixture was purified directly by reverse phase chromatography (C-18 silica from Waters, water/1:1 acetonitrile-methanol as eluents 0% to 100%). After purification were obtained 139 mg of tert-butyl 9-(2-(3-chloro-2-(pyridin-4-ylcarbamoyl)-1H-pyrrol-1-ylamino)-2-oxoethyl)-9H-purin-6-ylcarbamate (93% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09340547B2
出典データセットuspto-grants-2016_05
ORD IDord-bb4ce3d52fed455798ec7d2d727aeb89
出典メモuspto-grants-2016_05