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HRID 493124作成日:2026年10月25日

Potassium Carbonate → 4-tert-Butyloxycarbonylamino-1-(6-methoxy-[1,5]naphthyridin-4-yl)aminocarbonylpiperidine

https://huagongshe.com/reaction/493124

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物4-(tert-Butoxycarbonylamino)piperidine hydrochlorideHCID 2756028—
反応物6-Methoxy-1,5-naphthyridin-4-amineHCID 11435236—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒ChloroformHCID 6212—
生成物4-tert-Butyloxycarbonylamino-1-(6-methoxy-[1,5]naphthyridin-4-yl)aminocarbonylpiperidineHCID 22281715—

反応手順

To a solution of 4-amino-6-methoxy-[1,5]naphthyridine (Example 400a) (2.1 g, 13.5 mmol) and 4-(dimethylamino)pyridine (1.62 g) in anhydrous chloroform (45 ml) was added N,N-carbonyldiimidazole (3.28 g, 20.1 mmol). The mixture was stirred for 4 h at room temperature, then evaporated and the residue was dissolved in anhydrous DMF (45 ml). 4-tert-Butoxycarbonylaminopiperidine hydrochloride (3.34 g, 13.5 mmol) and potassium carbonate (1.89 g) were added, and the mixture was heated at 70° C. overnight. The mixture was evaporated and the residue was mixed with water (120 ml). The solid was filtered off and dried (3.89 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07534793B2
出典データセットuspto-grants-2009_05
ORD IDord-0004a56d53d64d0baae3855f59176ad0
出典メモuspto-grants-2009_05