돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2237630생성일: 2026년 10월 27일

Ethyl Acetate → 4-Amino-6-(4-iodophenyl)-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-5(6H)-one

https://huagongshe.com/reaction/2237630

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물N,N-Diethyl-2-propanamineHCID 521913—
반응물4,6-Dichloro-pyrimidine-5-carbonyl chlorideHCID 12163360—
반응물N-(2-{[tert-Butyl(dimethyl)silyl]oxy}ethyl)-4-iodoanilineHCID 59302533—
용매HeptaneHCID 8900—
용매HCID 178508906HCID 178508906—
생성물4-Amino-6-(4-iodophenyl)-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-5(6H)-oneHCID 59302530—

반응 단계

To a cooled (ice/water), stirred solution of N-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-4-iodoaniline (1.34 g, 2.78 mmol) and diethylisopropylamine (0.7 mL, 4.0 mmol) in MTHF (5 mL) was added 4,6-dichloroprimidine-5-carbonyl chloride (560 mg, 2.65 mmol). After 5 minutes, the cooling bath was removed and the slurry was stirred for 5 hours. Aqueous hydrochloric acid (1N, 5 mL) was added and the mixture was allowed to stand for 72 hours. The layers were separated and the aqueous layer was washed with MTHF (2×). The combined organic layers were washed with saturated aqueous sodium bicarbonate, saturated aqueous brine, dried over sodium sulfate and concentrated in vacuo to afford an oil. Chromatography (40 g silica gel column, 20-100% EtOAc:heptane) afforded the title compound, 542 mg. 1H NMR (400 MHz, CDCl3) δ 8.64 (s, 1H), 7.62 (d, 2H), 7.17 (d, 2H), 4.07 (t, 2H), 3.91 (q, 2H). m/z=438.0 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07718645B2
출처 데이터셋uspto-grants-2010_05
ORD IDord-76521802846e4ca3acc1f88eb4436c47
출처 메모uspto-grants-2010_05