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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1621776생성일: 2026년 10월 26일

Benzeneethanamine, alpha-methyl-, phosphate (1:1) → 4-(5-(Benzyloxy)-2-fluoropyridin-3-YL)-N,N-bis(4-methoxybenzyl)-6-methyl-1,3,5-triazin-2-amine

https://huagongshe.com/reaction/1621776

반응식

참여 물질

역할이름HCID투입량
반응물Benzeneethanamine, alpha-methyl-, phosphate (1:1)HCID 62885—
반응물Potassium AcetateHCID 517044—
반응물4-chloro-N,N-bis(4-methoxybenzyl)-6-methyl-1,3,5-triazin-2-amineHCID 59548209—
반응물5-(Benzyloxy)-2-fluoropyridin-3-ylboronic acidHCID 66599992—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물4-(5-(Benzyloxy)-2-fluoropyridin-3-YL)-N,N-bis(4-methoxybenzyl)-6-methyl-1,3,5-triazin-2-amineHCID 6659998741.8%

반응 조건

온도100 °C

반응 단계

A mixture of 4-chloro-N,N-bis(4-methoxybenzyl)-6-methyl-1,3,5-triazin-2-amine (0.150 g, 0.390 mmol), 5-(benzyloxy)-2-fluoropyridin-3-ylboronic acid (0.107 g, 0.432 mmol), Amphos (Aldrich) (0.014 g, 0.020 mmol), potassium acetate (Strem) (0.119 g, 1.22 mmol), EtOH (3 mL), and water (0.3 mL) was sealed under N2 and heated in a microwave at 100° C. for 20 min. The reaction mixture was partitioned between EtOAc and water. The aqueous layer was extracted with EtOAc (2×10 mL). The combined organic layers were dried over MgSO4 and concentrated. The crude product was purified by column chromatography (40 g, 10% to 20% EtOAc in hexanes) to give the product as a white solid (0.090 g). m/z (ESI, +ve ion) 552.0 (M+H)+. 1H NMR (300 MHz, CDCl3) δ 8.17 (d, J=7.31 Hz, 1H); 8.01 (br. s., 1H); 7.31-7.48 (m, 5H); 7.23 (d, J=7.89 Hz, 4H); 6.87 (t, J=7.60 Hz, 4H); 5.13 (s, 2H); 4.81 (d, J=6.28 Hz, 3H); 3.81 (d, J=8.33 Hz, 6H); 2.55 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08772480B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-a8cec71d571d4ae78b3cd655a621962f
출처 메모uspto-grants-2014_07