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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 419850생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/419850

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethoxyacetic acidHCID 12301—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물tert-Butyl 4-(hydrazinecarbonyl)piperidine-1-carboxylateHCID 22713165—
용매DimethylformamideHCID 6228—
생성물tert-Butyl 4-{[2-(ethoxyacetyl)hydrazino]carbonyl}piperidine-1-carboxylateHCID 59347451—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093400B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-550260baae444d04aaa2bb4b4d2ba678
출처 메모uspto-grants-2012_01