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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32364생성일: 2026년 10월 24일

Acetonitrile → 2-{4-Methyl-5-[2-(3-nitro-phenylamino)-pyrimidin-4-yl]-thiazol-2-ylamino}-ethanol

https://huagongshe.com/ko/reaction/32364

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물4-(2-Amino-4-methyl-5-thiazolyl)-N-(3-nitrophenyl)-2-pyrimidinamineHCID 447961—
반응물HCID 17859945HCID 17859945—
반응물Tert-butylimino-2-diethylamino-1,3-dimethylperhydro-1,3-diazaphosphorineHCID 69196119—
용매DimethylformamideHCID 6228—
용매Trifluoroacetic acidHCID 6422—
생성물2-{4-Methyl-5-[2-(3-nitro-phenylamino)-pyrimidin-4-yl]-thiazol-2-ylamino}-ethanolHCID 10109809—

반응 조건

온도124 °C

반응 단계

To a mixture of [4-(2-amino-4-methyl-thiazol-5-yl)-pyrimidin-2-yl]-(3-nitro-phenyl)-amine (0.33 g, 1.0 mmol) and iodoethanol (0.44 g, 2.6 mmol) in dry DMF (2 mL) was added tert-butylimino-2-diethylamino-1,3-dimethylperhydro-1,3-diazaphosphorine (0.5 mL). The reaction mixture was heated at 124° C. for 20 h. The product was isolated as a brown solid by preparative RP-HPLC (Vydac 218TP1022, 9 mL/min) using a gradient from 10-70% MeCN in 0.1% aq CF3COOH over 40 min. Anal. RP-HPLC: tR=14.30 min (Vydac 218TP54, 0-60% MeCN in 0.1% aq CF3COOH over 20 min, 1 mL/min, 25° C., purity >97%). 1H-NMR (CD3OD) δ: 3.30 (s, 3H, CH3), 3.91 (t, 2H, J=4.6 Hz, CH2), 4.25 (t, 2H, J=4.6 Hz, CH2), 7.21(d, 1H, J=5.2 Hz, pyrimidinyl-H), 7.54 (m, 1H, Ph-H), 7.89 (m, 2H, Ph-H), 8.59 (d, 1H, J=5.2 Hz, pyrimidinyl-H), 8.90 (s, 1H, Ph-H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07427627B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-180275eddee24ecfad2c9fbdc01cfca1
출처 메모uspto-grants-2008_09