돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 532893생성일: 2026년 10월 24일

Ammonia → Methyl 2-(5-iodo-3,4-dihydroisoquinolin-1-yl)propanoate

https://huagongshe.com/ko/reaction/532893

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Hydrochloric AcidHCID 313—
반응물Oxalyl chlorideHCID 65578—
반응물Sulfuric acid methanolHCID 18363649—
반응물Methyl 3-((2-iodophenethyl)amino)-2-methyl-3-oxopropanoateHCID 86711343—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물Methyl 2-(5-iodo-3,4-dihydroisoquinolin-1-yl)propanoateHCID 8671134412.2%

반응 단계

A solution of methyl 3-((2-iodophenethyl)amino)-2-methyl-3-oxopropanoate (9.9 g, 27.4 mmol) in DCM (120 mL) was treated with oxalyl chloride (2.59 mL, 30.2 mmol) and the mixture was stirred at RT for 30 min. FeCl3 (5.34 g, 32.9 mmol) was then added portionwise at 0° C. and the resulting brown mixture was stirred at RT for 4 h. A 2N aqueous solution of HCl (35 mL) was then added and the mixture was stirred at RT for another 2 h. The mixture was then diluted with H2O and extracted with DCM. The combined org. phases were then dried over Na2SO4, filtered and concentrated in vacuo. The brown residue obtained was taken up in a 19:1 mixture of MeOH/H2SO4 (120 mL) and stirred at reflux for 3 h. The mixture was then concentrated in vacuo and the brown reside obtained was taken up in H2O. The mixture was rendered basic with ammonia and then extracted with AcOEt. The combined org. phases were dried over Na2SO4, filtered and concentrated in vacuo. Purification by flash chromatography (SiO2, cHex/AcOEt 100:0 to 70:30) gave the title compound (1.15 g) as yellow oil. UPLC-MS: MS 344.1 (M+H+); UPLC rt 0.96 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853203B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-0ca03d1b97484d15b3676085b7b7a6ac
출처 메모uspto-grants-2014_10