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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1097611생성일: 2026년 10월 26일

Acetic Acid → HCID 86626310, 화합물

https://huagongshe.com/reaction/1097611

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물p-Toluenesulfonic acidHCID 6101—
반응물N4-Isobutyl-1,5-naphthyridine-3,4-diamineHCID 53699038—
반응물1,3-dimethoxycarbonyl-O-methylisoureaHCID 85348789—
용매MethanolHCID 887—
생성물HCID 86626310HCID 86626310—

반응 단계

A mixture of N4-(2-methylpropyl)[1,5]naphthyridine-3,4-diamine (Gerster et al, U.S. Pat. No. 6,194,425, Example 30 Part A, 4.10 g, 19.0 mmol), 1,3-dimethoxycarbonyl-O-methylisourea (7.21 g, 37.9 mmol), acetic acid (5.69 g, 94.8 mmol), and p-toluenesulfonic acid (3.60 g, 19.0 mmol) in methanol (50 mL) was heated at reflux for 16 hours. The volatiles were removed under reduced pressure, and the residue was dissolved in chloroform (150 mL). The solution was washed sequentially with water (150 mL), aqueous sodium carbonate (150 mL of 4% w/w), water (150 mL), and brine (150 mL) and then concentrated under reduced pressure. The residue was purified by automated flash chromatography (40+M silica cartridge, eluting with 0% to 20% CMA in chloroform) followed by recrystallization from acetonitrile to provide 1.78 g of methyl [1-(2-methylpropyl)-1H-imidazo[4,5-c][1,5]naphthyridin-2-yl]carbamate as a white solid, mp 195-197° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08143270B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-6678059f397a435994898fa220c42068
출처 메모uspto-grants-2012_03