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HRID 532893作成日:2026年10月26日

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

https://huagongshe.com/reaction/532893

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Hydrochloric AcidHCID 313—
反応物Oxalyl chlorideHCID 65578—
反応物Sulfuric acid methanolHCID 18363649—
反応物Methyl 3-((2-iodophenethyl)amino)-2-methyl-3-oxopropanoateHCID 86711343—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物Methyl 2-(5-iodo-3,4-dihydroisoquinolin-1-yl)propanoateHCID 8671134412.2%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08853203B2
出典データセットuspto-grants-2014_10
ORD IDord-0ca03d1b97484d15b3676085b7b7a6ac
出典メモuspto-grants-2014_10