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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 428980생성일: 2026년 10월 25일

Triethylamine → HCID 22141259, 화합물

https://huagongshe.com/reaction/428980

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-(Benzodioxol-5-yl)propionic acidHCID 64810—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물N-[3-(6-methyl-3-azabicyclo[3.1.0]hex-6-yl)phenyl)methanesulfonamideHCID 22141143—
용매DimethylformamideHCID 6228—
생성물AmmoniaHCID 222—
생성물HCID 22141259HCID 2214125939%

반응 단계

To a solution of 3-(1,3-benzodioxol-5-yl)propanoic acid (120 mg, 0.62 mmol) in N,N-dimethylformamide (13 ml) was added 1-hydroxybenzotriazole monohydrate (100 mg, 0.66 mmol) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (170 mg, 0.88 mmol). After stirring at room temperature for 5 min the mixture was treated with the hydrochloride salt of N-[3-(6-methyl-3-azabicyclo[3.1.0]hex-6-yl)phenyl]methanesulfonamide (Preparation 53, 200 mg, 0.66 mmol) and triethylamine (133 mg, 1.32 mmol). The reaction mixture was stirred at room temperature for 72 h before concentrating in vacuo. Water (10 ml) was added and the reaction mixture was extracted with ethyl acetate (2×15 ml). The combined organic extracts were washed with water (10 ml) and saturated brine (10 nml), dried (Na2SO4), filtered and concentrated in vacuo to give a light brown oil. The residue was purified by chromatography using a Sep-Pak™ cartridge packed with silica gel (10 g) eluting with dichloromethane:ethanol: 0.88 ammonia (300:8:1) to afford the title compound as a white foam (107 mg, 38%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313312B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-ac32867ce25c4c88b3ee395b803523df
출처 메모uspto-grants-2001_11