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HRID 81946作成日:2026年10月26日

Iodine → ethyl 8-iodo-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate

https://huagongshe.com/reaction/81946

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Isoamyl NitriteHCID 8053—
反応物Cesium iodideHCID 24601—
反応物ethyl 8-amino-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylateHCID 24993827—
触媒Copper iodideHCID 83717—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物ethyl 8-iodo-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylateHCID 4423294346%

反応手順

To a well stirred suspension of ethyl 8-amino-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate (9.0 g, 33 mmol) in dimethoxyethane (0.7 L) under N2, cesium iodide (8.6 g, 33 mmol), bisublimated iodine (4.19 g, 16.5 mmol), copper iodide (2.0 g, 10 mmol) and isopentyl nitrite (6.62 mL, 49.5 mmol) were added in sequence. The reaction mixture was stirred vigorously at 65-70° C. for 3 hours. After cooling in an ice-water bath, the solid was filtered off. The filtrate was diluted with dichloromethane (2.0 L), washed with 30% ammonium hydroxide (150 mL), sodium thiosulphate (300 mL), brine, dried over anhydrous Na2SO4 and concentrated to give 5.69 g of the title compound (46% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846701B2
出典データセットuspto-grants-2014_09
ORD IDord-bc92d3892c64466fa8b33352c03f5173
出典メモuspto-grants-2014_09