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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2364617생성일: 2026년 10월 26일

Sodium Carbonate → (1E,4E)-ethyl 2-amino-8-(3-morpholinopropyl)-3H-benzo[b]azepine-4-carboxylate

https://huagongshe.com/reaction/2364617

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참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물Cesium carbonateHCID 10796—
반응물4-Bromo-2-nitrobenzaldehydeHCID 608099—
반응물(4-(Pyrrolidine-1-carbonyl)phenyl)boronic acidHCID 2773571—
반응물Ethyl 8-bromo-2-((tert-butoxycarbonyl)amino)-3H-benzo[b]azepine-4-carboxylateHCID 58228529—
반응물4-(3-(9-Borabicyclo[3.3.1]nonan-9-yl)propyl)morpholineHCID 66961487—
반응물3-Nitro-4'-(pyrrolidine-1-carbonyl)biphenyl-4-carbaldehydeHCID 86652678—
촉매HCID 178418397HCID 178418397—
용매EthanolHCID 702—
용매TolueneHCID 1140—
용매Ethanol toluene waterHCID 86587398—
생성물(1E,4E)-ethyl 2-amino-8-(3-morpholinopropyl)-3H-benzo[b]azepine-4-carboxylateHCID 50943695—

반응 조건

온도100 °C

반응 단계

The title compound was prepared by these procedures using (1E,4E)-ethyl 8-bromo-2-(tert-butoxycarbonylamino)-3H-benzo[b]azepine-4-carboxylate and 4-(3-(9-borabicyclo[3.3.1]nonan-9-yl)propyl)morpholine. Preparation of 3-nitro-4′-(pyrrolidine-1-carbonyl)biphenyl-4-carbaldehyde, except in this case a co-solvent of EtOH/toluene/water (2:1:1) and Cs2CO3 were used: To a solution of 4-bromo-2-nitrobenzaldehyde (20.2 g, 87.9 mmol), 4-(pyrrolidine-1-carbonyl)phenylboronic acid (21.2 g, 96.7 mmol), and Pd(PPh3)4 (508 mg, 0.440 mmol) in toluene (200 mL) was added EtOH (40 mL) followed by Na2CO3 (70.0 mL, 140 mmol, 2 M aq solution) at room temperature. The resulting mixture was heated at 100° C. for 18 h. The reaction mixture was cooled to room temperature and the organic layer was separated. The aqueous layer was extracted with EtOAc (300 mL). The combined organic layers were washed with brine (500 mL), dried over MgSO4, filtered, and concentrated under reduced pressure to give the crude material that was combined with another batch of the crude material obtained from an additional run in the same reaction scale. The combined crude material was purified by silica gel flash column chromatography (CH2Cl2 to 1% MeOH in CH2Cl2). Preparation of (1E,4E)-2-amino-N-(2-amino-2-oxoethyl)-N-propyl-8-(4-(pyrrolidine-1-carbonyl)phenyl)-3H-benzo[b]azepine-4-carboxamide: A solution of the crude tert-butyl (1E,4E)-4-((2-amino-2-oxoethyl)(propyl)carbamoyl)-8-(4-(pyrrolidine-1-carbonyl)phenyl)-3H-benzo[b]azepin-2-ylcarbamate in anhydrous CH2Cl2 (15 mL) was bubbled with HCl (gas) for 4 h at 0° C. The resulting mixture was warmed to room temperature and stirred until the reaction was complete. To this mixture was added saturated NaHCO3 at 0° C. The aqueous layer was separated and extracted with CH2Cl2. The combined organic layers were dried over Na2SO4, filtered, and concentrated under reduced pressure to give the crude compound that was purified by silica gel flash column chromatography (MeOH:CH2Cl2=1:50).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08691809B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-bf50740ae9bf4c73b9f919666e46195d
출처 메모uspto-grants-2014_04