돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 528920생성일: 2026년 10월 26일

ethyl 4-bromo-5-methyl-1H-pyrazole-3-carboxylate → 4-bromo-N,N-dibutyl-5-methyl-1H-pyrazole-3-carboxamide

https://huagongshe.com/reaction/528920

반응식

참여 물질

역할이름HCID투입량
반응물ethyl 4-bromo-5-methyl-1H-pyrazole-3-carboxylateHCID 616098—
반응물N,N-dibutyl-4-chloro-5-methyl-1H-pyrazole-3-carboxamideHCID 71062189—
생성물4-bromo-N,N-dibutyl-5-methyl-1H-pyrazole-3-carboxamideHCID 4737016375%

반응 단계

Following a procedure analogous to that for the synthesis of Intermediate 1B, ethyl 4-bromo-5-methyl-1H-pyrazole-3-carboxylate (Tabrizi, M. A. et al., Bioorg. Med. Chem., 16:2419-2430 (2008)) (5.68 g, 24.4 mmol) was converted to the title compound (5.79 g, 75%). 1H NMR (CDCl3) δ 3.51 (t, J=7.4 Hz, 2H), 3.38-3.26 (m, 2H), 2.34 (s, 3H), 1.73-1.34 (m, 6H), 1.22-1.13 (m, 2H), 1.03-0.75 (m, 6H); MS(ESI+) m/z 316.2 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09346795B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-f623520f9c7149d39e8e4bea76b97e97
출처 메모uspto-grants-2016_05