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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1696428생성일: 2026년 10월 25일

1,2-Dichloro-3-isocyanatobenzene → ethyl 4-{3-t-butyl-5-[3-(2,3-dichlorophenyl)-ureido]-1H-pyrazol-1-yl}benzoate

https://huagongshe.com/reaction/1696428

반응식

참여 물질

역할이름HCID투입량
반응물1,2-Dichloro-3-isocyanatobenzeneHCID 33050—
반응물Pentanenitrile, 4,4-dimethyl-3-oxo-HCID 108871—
반응물Ethyl 4-hydrazinylbenzoateHCID 792992—
반응물ethyl 4-(3-t-butyl-5-amino-1H-pyrazol-1-yl)benzoateHCID 12044795—
생성물ethyl 4-{3-t-butyl-5-[3-(2,3-dichlorophenyl)-ureido]-1H-pyrazol-1-yl}benzoateHCID 5885125748%

반응 단계

Using General method A, ethyl 4-(3-t-butyl-5-amino-1H-pyrazol-1-yl)benzoate (1 g, 3.09 mmol, prepared from ethyl 4-hydrazinobenzoate and pivaloylacetonitrile by the procedure of Regan, et al., J. Med. Chem., 45, 2994 (2002)) and 1,2-dichloro-3-isocyanato-benzene (0.7 g, 3.71 mmol) were combined to afford ethyl 4-{3-t-butyl-5-[3-(2,3-dichlorophenyl)-ureido]-1H-pyrazol-1-yl}benzoate (0.7 g, 48% yield). 1H NMR (300 MHz, DMSO-d6): δ 9.20 (brs, 1H), 8.77 (brs, 1H), 8.04 (m, 1H), 7.44 (brs, 4H), 7.29-7.26 (m, 2H), 6.36 (s, 1H), 4.31 (q, J=7.2 Hz, 2H), 1.27 (s, 9H), 1.26 (t, J=7.2 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08163756B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-6e4af1ba9def40e9a0b95c5acc9639e9
출처 메모uspto-grants-2012_04