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HRID 432186作成日:2026年10月25日

Sodium Carbonate Monohydrate → HCID 178480957、化合物

https://huagongshe.com/reaction/432186

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Tert-butyl n-{phenyl[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl}carbamateHCID 22347089—
反応物HCID 178481014HCID 178481014—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物HCID 178480957HCID 17848095769.4%

反応手順

A mixture of tert-butyl N-{phenyl[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl}carbamate (3.0 g,0.00733 mol), cis-3-iodo-1-[4-(4-methylpiperazino)-cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-4-amine (2.4 g, 0.0054 mol), tetrakis-(triphenylphosphine)palladium (0.381 g, 0.00033 mol) and sodium carbonate monohydrate (1.69 g, 0.0136 mol) was heated in a mixture of ethylene glycol dimethyl ether (80 mL) and water (40 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 partitioned between saturated aqueous sodium bicarbonate solution (200 mL) and ethyl acetate (200 mL), the organic layer separated and the aqueous layer further extracted with ethyl acetate twice (100 mL each). The combined organic extracts were dried over magnesium sulfate. The solvents were evaporated under reduced pressure to leave a tan solid which was purified by flash column chromatography on silica using dichloromethane/triethylamine/methanol (96:3:1) as a mobile phase to give cis-tert-butyl N-[(4-{4-amino-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}phenyl)(phenyl)-methyl]carbamate (2.24 g, 0.00375 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-14edba70573b4d0697b95476b79f796e
出典メモuspto-grants-2003_12