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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 872306생성일: 2026년 10월 26일

Diisopropylethylamine → {1-[4-(6-Bromo-8-methyl-3-phenyl-imidazo[1,2-a]pyridin-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/872306

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물2-Amino-5-bromo-3-methylpyridineHCID 137934—
반응물tert-Butyl (1-{4-[bromo(phenyl)acetyl]phenyl}cyclobutyl)carbamateHCID 86691038—
용매IsopropanolHCID 3776—
생성물{1-[4-(6-Bromo-8-methyl-3-phenyl-imidazo[1,2-a]pyridin-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl esterHCID 6666512817.2%

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온도130 °C

반응 단계

1.25 g (2.81 mmol) {1-[4-(2-Bromo-2-phenyl-acetyl)phenyl]-cyclobutyl}-carbamic acid tert.-butyl ester, 631.4 mg (3.38 mmol) 2-amino-5-bromo-3-methyl-pyridine, 2.15 g molecular sieves (4 Å, dried over night at 120° C. in a drying oven), 363.5 mg (2.81 mmol) N,N-diisopropylethylamine in 12 mL 2-propanol (degassed for 15′) in a microwave vial, sealed with a microwave cap, were heated at 130° C. for 17 hours in a heating block. The reaction mixture was sucked off via a glass fibre filter and the filter was washed with dichloromethane. After evaporation to dryness, the residue was redissolved in dichloromethane (200 mL), washed with an 1 M hydrochloric acid (50 mL), saturated sodium bicarbonate (50 mL) and brine (100 mL) and dried (sodium sulfate). After filtration and removal of the solvent the residue was purified by chromatography on silicagel (eluents: hexane/ethyl acetate) yielding 256.7 mg (17.1%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08975265B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-e83ab6a75d164371bda3cd6fc72d6af4
출처 메모uspto-grants-2015_03