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HRID 551906作成日:2026年10月26日

Dimethylformamide → Methyl [4-({{4-[(4-butylphenyl)ethynyl]benzyl}[(4-cyanoanilino)-carbonyl]amino}methyl)phenoxy]acetate

https://huagongshe.com/reaction/551906

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Tris(hydroxymethyl)aminomethaneHCID 6503—
反応物4-Cyanophenyl isocyanateHCID 170380—
反応物Methyl {4-[({4-[(4-butylphenyl)ethynyl]benzyl}amino)methyl]phenoxy}acetateHCID 57554567—
溶媒DichloromethaneHCID 6344—
生成物Methyl [4-({{4-[(4-butylphenyl)ethynyl]benzyl}[(4-cyanoanilino)-carbonyl]amino}methyl)phenoxy]acetateHCID 11621237132.1%

反応手順

To a solution of methyl {4-[({4-[(4-butylphenyl)ethynyl]benzyl}amino)methyl]-phenoxy}acetate (37 mg, 0.084 mmol) in anhydrous DCM (2 ml) was added 4-cyanophenyl isocyanate (Aldrich, 45 mg, 0.31 mmol) and the reaction mixture was stirred at rt for 18 hrs. Then PS-trisamine resin (75 mg, Novabiochem, 3.5 mmol/g) and DMF (1 mL) were added and the resulting mixture was stirred at rt for 5 additional hrs. Removal of the resin by filtration followed by evaporation of the solvents gave 65 mg (97%) of the title compound as a pale yellow oil. HPLC, Rt: 5.7 min (purity: 74.1%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07947851B2
出典データセットuspto-grants-2011_05
ORD IDord-b7fb90f33d7946b995f6784ce9ebb79e
出典メモuspto-grants-2011_05