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HRID 432328作成日:2026年10月27日

Sodium Carbonate Monohydrate → HCID 178476556、化合物

https://huagongshe.com/reaction/432328

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium Carbonate MonohydrateHCID 2735133—
反応物N-(2,3-dihydrobenzo[b]furan-3-yl)-N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]amineHCID 22346766—
反応物HCID 178481015HCID 178481015—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物HCID 178476556HCID 17847655691.3%

反応手順

A mixture of N-(2,3-dihydrobenzo[b]furan-3-yl)-N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]amine (0.089 g, 0.000265 mol), trans-3-iodo-1-[4-(4-methylpiperazino)-cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-4-amine (0.090 g, 0.000204 mol), tetrakis-(triphenylphosphine)palladium (0.014 g, 0.000012 mol) and sodium carbonate monohydrate (0.063 g, 0.00051 mol) was heated in a mixture of ethylene glycol dimethyl ether (5 mL) and water (3 mL) at 80° C. for sixteen hours under an atmosphere of nitrogen. The mixture was allowed to cool to ambient temperature and solvents were removed under the reduced pressure. The residue was purified by preparative HPLC (Hypersil C18, 8 μm, 25 cm; 10-60% acetonitrile-0.1M ammonium acetate over 25 min, 21 mL/min) to yield trans-3-[4-(2,3-dihydrobenzo[b]furan-3-ylamino)phenyl]-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-4-amine diacetate (0.078 g, 0.000121 mol) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06660744B1
出典データセットuspto-grants-2003_12
ORD IDord-13894ac1b4954b71980879148d2a2144
出典メモuspto-grants-2003_12