돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 442098생성일: 2026년 10월 25일

Acetic Acid → 2-[2-(1-Methoxyethylideneamino)-5-bromobenzoyl]pyridine

https://huagongshe.com/reaction/442098

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물BenzeneHCID 241—
반응물2-(2-Amino-5-bromobenzoyl)pyridineHCID 73807—
생성물2-[2-(1-Methoxyethylideneamino)-5-bromobenzoyl]pyridineHCID 21416619—

반응 단계

A mixture of 8.7 g of 2-(2-amino-5-bromobenzoyl)-pyridine, 5.7 g of ortho-methyl-acetate, 2.8 ml. of acetic acid and 100 ml. of benzene is refluxed, while removing alcohol formed by azeotropic distillation, for 1.5 hours and then cooled. The resultant is washed with saturated aqueous sodium hydrogen carbonate, then with water, and dried over sodium sulfate. Evaporation of the solvent under reduced pressure gives 2-[2-(1-methoxyethylideneamino)-5-bromobenzoyl]-pyridine as oily product. This product is dissolved in 60 ml. methanolic solution and 44 ml. of hydrazine hydrate (100%) and 1.9 ml. of acetic acid are added to the solution. The mixture is stirred at room temperature for 3 hours and the precipitate formed is collected by filtration, washed with methanol and dried to give 3-amino-6-bromo-3,4-dihydro-4-hydroxy-2-methyl-4-(2-pyridyl)quinazoline as crystals. Recrystallization from a mixture of methanol and chloroform gives colorless crystals, melting at 208° to 210° C (decomposition).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04044129
출처 데이터셋uspto-grants-1977_08
ORD IDord-d8dd0a936b7445459bd1cac12bb8b18d
출처 메모uspto-grants-1977_08