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HRID 474473作成日:2026年10月25日

Water → methyl 4-{[(3S)-1-(tert-butoxycarbonyl)piperidin-3-yl]amino}-6-iodoquinazoline-8-carboxylate

https://huagongshe.com/reaction/474473

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium HydroxideHCID 14798—
反応物tert-butyl (3S)-3-aminopiperidine-1-carboxylateHCID 1501975—
反応物Methyl 4-chloro-6-iodoquinazoline-8-carboxylateHCID 77231312—
溶媒AcetonitrileHCID 6342—
生成物methyl 4-{[(3S)-1-(tert-butoxycarbonyl)piperidin-3-yl]amino}-6-iodoquinazoline-8-carboxylateHCID 6676386814.3%

反応手順

Dissolved tert-butyl (35)-3-aminopiperidine-1-carboxylate (632.11 mg; 3.16 mmol; 1.10 eq.) in MeCN (18.00 ml) and TEA (1.00 ml). Added this mixture to methyl 4-chloro-6-iodoquinazoline-8-carboxylate (1000.00 mg; 2.87 mmol; 1.00 eq.). Stirred reaction at room temperature for 45 hours. LCMS indicated M+1=513 present. Diluted reaction with water and 1N NaOH. Filtered the resulting precipitate. Washed with water and dried to give a yellowish solid (210 mg). Carried material on without further purification. LCMS: M+1=513

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08637532B2
出典データセットuspto-grants-2014_01
ORD IDord-e86dd1e0306b49829c7fcbea9a8491cb
出典メモuspto-grants-2014_01