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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16945생성일: 2026년 10월 23일

alpha-Naphthyl isocyanate → 1-(3-Tert-butyl-1-(3-(2-morpholino-2-oxoethyl)phenyl)-1h-pyrazol-5-yl)-3-(naphthalen-1-yl)urea

https://huagongshe.com/ko/reaction/16945

반응식

참여 물질

역할이름HCID투입량
반응물alpha-Naphthyl isocyanateHCID 66589—
반응물2-[3-(3-t-butyl-5-amino-1H-pyrazol-1-yl)phenyl]-1-morpholinoethanoneHCID 21867345—
용매DichloromethaneHCID 6344—
생성물1-(3-Tert-butyl-1-(3-(2-morpholino-2-oxoethyl)phenyl)-1h-pyrazol-5-yl)-3-(naphthalen-1-yl)ureaHCID 21867339—

반응 단계

A mixture of Example L (0.2 g, 0.58 mmol) and 1-naphthylisocyanate (0.10 g, 0.6 mmol) in dry CH2Cl2 (4 ml) was stirred at RT under N2 for 18 h. The solvent was removed in vacuo and the crude product was purified by column chromatography using ethyl acetate/hexane/CH2Cl2 (3/1/0.7) as the eluent (0.11 g, off-white solid) to yield 1-{3-tert-butyl-1-[3-(2-morpholino-2-oxoethyl)phenyl]-1H-pyrazol-5-yl}-3-(naphthalene-1-yl)urea. mp: 194-196; 1H NMR (200 MHz, DMSO-d6): δ 9.07 (1H, s), 8.45 (s, 1H), 8.06-7.93 (m, 3H), 7.69-7.44 (m, 7H), 7.33-7.29 (d, 6.9 Hz, 1H), 6.44 (s, 1H), 3.85 (m, 2H), 3.54-3.45 (m, 8H), 1.31 (s, 9H); MS:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737283B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-3d6c2a70a5244194aac4fd5b3b2d9622
출처 메모uspto-grants-2010_06