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HRID 923660作成日:2026年10月25日

Propylphosphonic anhydride → (1-{4-Bromo-6-[(triisopropylsilanyl)-ethynyl]-pyridin-2-ylcarbamoyl}-ethyl)-methyl-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/923660

反応式

関与物質

役割名称HCID仕込み量
反応物Propylphosphonic anhydrideHCID 111923—
反応物Sodium BicarbonateHCID 516892—
反応物2-(((Tert-butoxy)carbonyl)(methyl)amino)propanoic acidHCID 4436857—
反応物4-Bromo-6-[2-[tris(propan-2-yl)silyl]ethynyl}pyridin-2-amineHCID 123389078—
溶媒PyridineHCID 1049—
溶媒Ethyl AcetateHCID 8857—
生成物(1-{4-Bromo-6-[(triisopropylsilanyl)-ethynyl]-pyridin-2-ylcarbamoyl}-ethyl)-methyl-carbamic acid tert-butyl esterHCID 123968434—

反応手順

2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphorinane-2,4,6-trioxide (70 ml of a 50 wt.-% solution in EtOAc, 118 mmol) is added to a mixture of 4-bromo-6-{2-[tris(propan-2-yl)silyl]ethynyl}pyridin-2-amine B1 (10.4 g, 29.5 mmol), 2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]propanoic acid (12 g, 59 mmol) and pyridine (20 ml) at −20° C. The mixture is stirred for 3 h at that temperature. 200 ml of a saturated aqueous sodium hydrogencarbonate solution is added and the mixture extracted with EtOAc. The combined organic layers are dried over MgSO4 and concentrated in vacuo. The product is purified by NP chromatography. Yield: 11.1 g (70%). HPLC-MS: M+H=538/540; tR=.2.05 min (METHOD—1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09278978B2
出典データセットuspto-grants-2016_03
ORD IDord-0d8322577e0848fcbf4e8f05bf79edc5
出典メモuspto-grants-2016_03