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HRID 419850作成日:2026年10月27日

Triethylamine → tert-Butyl 4-{[2-(ethoxyacetyl)hydrazino]carbonyl}piperidine-1-carboxylate

https://huagongshe.com/reaction/419850

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ethoxyacetic acidHCID 12301—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
反応物tert-Butyl 4-(hydrazinecarbonyl)piperidine-1-carboxylateHCID 22713165—
溶媒DimethylformamideHCID 6228—
生成物tert-Butyl 4-{[2-(ethoxyacetyl)hydrazino]carbonyl}piperidine-1-carboxylateHCID 59347451—

反応手順

A mixture of 4-hydrazinocarbonyl-piperidine-1-carboxylic acid tert-butyl ester (WO 2000039125, prep 27) (3 g, 12.33 mmol), ethoxyacetic acid (1.28 mL, 13.56 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (2.6 g, 13.56 mmol), 1-hydroxybenzotriazole hydrate (1.83 g, 13.56 mmol) and triethylamine (2.1 mL, 14.8 mmol) in N,N-dimethylformamide (15 mL) was stirred at room temperature for 18 hours. The mixture was concentrated under reduced pressure and the residue was partitioned between ethyl acetate and aqueous sodium carbonate solution. The layers were separated, the organic phase was dried over MgSO4 and evaporated under reduced pressure to provide the title compound as an oil, that crystallised on standing.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08093400B2
出典データセットuspto-grants-2012_01
ORD IDord-550260baae444d04aaa2bb4b4d2ba678
出典メモuspto-grants-2012_01