돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1797115생성일: 2026년 10월 26일

Chloroform → 3-[3-(3-Methoxypropyl)-5-(6-phenylpyridin-3-yl)-1,2,4-triazol-4-yl]-2-methylbenzamide

https://huagongshe.com/reaction/1797115

반응식

참여 물질

역할이름HCID투입량
반응물ChloroformHCID 6212—
반응물Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 18462—
반응물3-Amino-2-methylbenzamideHCID 16495773—
반응물5-[5-(3-Methoxypropyl)-1,3,4-oxadiazol-2-yl]-2-phenylpyridineHCID 22019236—
용매1,3-Dimethyl-2-imidazolidinoneHCID 6661—
생성물3-[3-(3-Methoxypropyl)-5-(6-phenylpyridin-3-yl)-1,2,4-triazol-4-yl]-2-methylbenzamideHCID 2201925156.1%

반응 조건

온도200 °C

반응 단계

5-[5-(3-Methoxypropyl)-1,3,4-oxadiazol-2-yl]-2-phenylpyridine (1.0 g) prepared in the Reference Example 7 was dissolved in 1,3-dimethyl-2-imidazolidinone (10 ml), followed by addition of 3-amino-2-methylbenzamide (1.53 g) prepared in the Reference Example 6 and D-10-camphorsulfonic acid (290 mg), and stirred at 200° C. for 16 hours. After the reaction solution was cooled to ambient temperature, chloroform was added to the solution, which was then washed with saturated aqueous sodium hydrogen carbonate solution. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: chloroform/methanol=10/1), to afford the entitled compound (812 mg, 56%). The physico-chemical values are as follows.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07034047B2
출처 데이터셋uspto-grants-2006_04
ORD IDord-1438de3a430e4ba0b28f430c64246fe1
출처 메모uspto-grants-2006_04