돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1711610생성일: 2026년 10월 27일

Sodium Chloride → methyl 1-benzyl-1H-indazole-3-carboxylate

https://huagongshe.com/reaction/1711610

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물Benzyl BromideHCID 7498—
반응물Sodium hydrideHCID 24758—
반응물methyl 1H-indazole-3-carboxylateHCID 657476—
용매TetrahydrofuranHCID 8028—
생성물methyl 1-benzyl-1H-indazole-3-carboxylateHCID 1056369084%

반응 조건

온도25 °C

반응 단계

Sodium hydride (0.37 g. 60%, 9.3 mmol) was added to a solution of indazole-3-carboxylic acid methyl ester (1.5 g, 8.5 mmol) in dry THF (50 mL) at 0° C. Benzyl bromide (1.59 g, 9.3 mmol) was then added and the reaction mixture was warmed to 25° C. and stirred for 8 h The reaction mixture was poured onto saturated NaCl solution (100 mL) and extracted with 3×200 mL of diethyl ether. The combined extracts were dried (MgSO4) and concentrated under reduced pressure. The crude compound was purified by flash chromatography using cyclohexane/ethyl acetate (70:30) and recrystallised from cyclohexane/ethyl acetate to afford the title compound as a yellow solid (1.89 g, 84%). Mp 72-73° C. 1H NMR (300 MHz, CDCl3) ppm 4.07 (s, 3H), 5.72 (s, 2H), 7.22-7.40 (m, 8H), 8.24-8.27 (m, 1H). MS(EI) m/z 266 [M+]. Anal. Calcd. for C16H14N2O2: C, 72.17; H, 5.30; N, 10.52. Found: C, 72.12; H, 5.15; N, 10.85.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07790761B2
출처 데이터셋uspto-grants-2010_09
ORD IDord-cabcf39df2964ceab60afc0f592e5fb8
출처 메모uspto-grants-2010_09