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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 448123생성일: 2026년 10월 25일

Methanol → 4-Chloro-2-[1,2,4]triazolo[4,3-a]pyrimidin-3-yl-phenylamine

https://huagongshe.com/reaction/448123

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물5-Chloro-2-nitrobenzaldehydeHCID 81123—
반응물2-HydrazinylpyrimidineHCID 346558—
반응물Iodo benzene diacetateHCID 12217721—
촉매IronHCID 23925—
용매EthanolHCID 702—
용매Ammonium ChlorideHCID 25517—
생성물4-Chloro-2-[1,2,4]triazolo[4,3-a]pyrimidin-3-yl-phenylamineHCID 43628644—

반응 조건

온도60 °C

반응 단계

A 5 mL scintillation vial was charged with 2-hydrazinopyrimidine (61 mg, 0.55 mmol), 2-nitro-5-chlorobenzaldehyde (112 mg, 0.60 mmol) and MeOH (500 μL) and heated to 60° C. for 30 minutes. The MeOH was then removed in vacuo and the resultant solid was washed with Et2O. The crude solid (30 mg) was then suspended in CH2Cl2 (1 mL) and iodobenzene diacetate (39 mg, 0.12 mmol) was added. The reaction was stirred at room temperature for 30 minutes after which the solvent was removed in vacuo. The resultant residue was then dissolved in a 10% solution of saturated NH4Cl(aq) in EtOH and iron (19 mg, 0.33 mmol) was then added and the reaction was stirred at 80° C. for 4 h. The solvent was then removed in vacuo and the product was purified by silica gel chromatography to afford 4-chloro-2-[1,2,4]triazolo[4,3-a]pyrimidin-3-yl-phenylamine as a light yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481579B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-0b6bc742720c489698823c3cb82c3e17
출처 메모uspto-grants-2013_07