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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1478239생성일: 2026년 10월 25일

Methylamine → 2-Methoxy-5-(methylaminocarbonyl)phenylboronic acid

https://huagongshe.com/reaction/1478239

반응식

참여 물질

역할이름HCID투입량
반응물MethylamineHCID 6329—
반응물4-MethylmorpholineHCID 7972—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물5-Carboxy-2-methoxybenzeneboronic acidHCID 42614541—
용매DimethylformamideHCID 6228—
생성물2-Methoxy-5-(methylaminocarbonyl)phenylboronic acidHCID 5749732456.9%

반응 단계

3-Borono-4-methoxybenzoic acid (2.5 g, 12.50 mmol) was dissolved in DMF (6 ml) and 12.50 ml methylamine (2 M solution in THF, 25 mmol) was added followed by HATU (4.75 mg, 12.5 mmol) and NMM (1.375, 12.50 mmol). The reaction mixture was stirred at RT for 20 hours and concentrated. The crude material was added to 50 ml water and extracted 3 times with EtOAc. The combined organic phases were dried (Na2SO4), filtered and concentrated. The crude material was triturated in EtOAc and filtered. The residue was purified by chromatography (Silicagel, CH2Cl2/MeOH 95:5) to give 1.92 g (7.11 mmol, 56.9% yield) of the title compound as a colorless solid. LCMS: (M+H)=210; tR=0.50 min (LC-MS 1). TLC: Rf=0.27 (CH2Cl2/MeOH 95:5). HPLC: tR=3.76 min (HPLC 3). 1H-NMR (d6-DMSO, 600.13 MHz) δ ppm 8.29 (bs, 1H), 8.03 (s, 1H), 7.87 (d, 1H), 7.85 (s, 2H) 7.02 (d, 1H), 3.84 (s, 3H), 2.75 (d, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09403827B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-87687641b35449b98adf98e5ebec1704
출처 메모uspto-grants-2016_08