돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1088397생성일: 2026년 10월 24일

Potassium Iodide → cis-4-amino-5-chloro-N-[1-[2-(1,4-dihydro-2,4-dioxo-3(2H)-quinazolinyl)ethyl]-3-methoxy-4-piperidinyl]-2-methoxybenzamide

https://huagongshe.com/ko/reaction/1088397

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물3-(2-chloroethyl)(1H,3H)quinazoline-2,4-dioneHCID 78766—
반응물Sodium BicarbonateHCID 516892—
반응물4-Amino-5-chloro-2-methoxy-N-[(3R,4S)-3-methoxypiperidin-4-YL]benzamideHCID 9861621—
용매WaterHCID 962—
용매Methyl Isobutyl KetoneHCID 7909—
생성물cis-4-amino-5-chloro-N-[1-[2-(1,4-dihydro-2,4-dioxo-3(2H)-quinazolinyl)ethyl]-3-methoxy-4-piperidinyl]-2-methoxybenzamideHCID 15096932—

반응 단계

A mixture of 3.8 parts of 3-(2-chloroethyl)-2(1H), 4(3H)-quinazolinedione, 4.7 parts of cis-4-amino-5-chloro-2-methoxy-N-(3-methoxy-4-piperidinyl)benzamide, 1.7 parts of sodium hydrogen carbonate, 0.1 parts of potassium iodide and 160 parts of 4-methyl-2-pentanone was stirred and refluxed for 24 hours. Water was added to the reaction mixture. The precipitated product was filtered off and crystallized from N,N-dimethylformamide and a small amount of water, yielding 3.3 parts of cis-4-amino-5-chloro-N-[1-[2-(1,4-dihydro-2,4-dioxo-3(2H)-quinazolinyl)ethyl]-3-methoxy-4-piperidiny]-2-methoxybenzamide; mp. 270.8° C. (compound 142).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04962115
출처 데이터셋uspto-grants-1990_10
ORD IDord-022d02862e7943faa08f947abacb089a
출처 메모uspto-grants-1990_10