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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 498005생성일: 2026년 10월 26일

3-(Chloromethyl)pyridine → 2-[[3-Methyl-1-(3-pyridinylmethyl)-1H-pyrazol-5-yl]amino]benzoic acid

https://huagongshe.com/reaction/498005

반응식

참여 물질

역할이름HCID투입량
반응물3-(Chloromethyl)pyridineHCID 18358—
반응물Pyridin-3-ylmethyl-hydrazineHCID 12232495—
반응물2-(2-Oxo-propyl)-benzo[D][1,3]oxazin-4-oneHCID 15938097—
용매EthanolHCID 702—
생성물2-[[3-Methyl-1-(3-pyridinylmethyl)-1H-pyrazol-5-yl]amino]benzoic acidHCID 2232020567%

반응 단계

A solution in ethanol (50 mL) of 2-(2-oxopropyl)-4H-3,1-benzoxazin-4-one (11.2 g, 55.1 mmol) and 3-hydrazinomethylpyridine (7.44 g, 60.4 mmol) which was prepared from 3-chloromethylpyridine following the method described in Reference Example 2-2, was heated under reflux for 1 hour. The solution was cooled to room temperature, and the resulting crude crystals were collected by filtration. The crystals were washed with ethanol and air dried to give the title compound (11.3 g, 67% yield). mp: 180-183° C. (recrystallized from ethanol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06949648B2
출처 데이터셋uspto-grants-2005_09
ORD IDord-cf44457fb6344e3fba6132667320dab9
출처 메모uspto-grants-2005_09