戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 38465作成日:2026年10月23日

Pyridine → Methyl 4-(3-methyl-6-{[6-(1-methyl-1H-pyrazol-4-yl)-4-oxospiro[chroman-2,4'-piperidin]-1'-yl]carbonyl}-1H-indazol-1-yl)benzoate

https://huagongshe.com/ja/reaction/38465

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物4-Methoxycarbonylphenylboronic acidHCID 2734369—
反応物HCID 178434311HCID 178434311—
触媒Cupric acetateHCID 8895—
溶媒DichloromethaneHCID 6344—
生成物Methyl 4-(3-methyl-6-{[6-(1-methyl-1H-pyrazol-4-yl)-4-oxospiro[chroman-2,4'-piperidin]-1'-yl]carbonyl}-1H-indazol-1-yl)benzoateHCID 58208718—

反応手順

Pyridine (0.080 ml, 0.988 mmol) was added to a stirred mixture of 1′-[(3-methyl-1H-indazol-6-yl)carbonyl]-6-(1-methyl-1H-pyrazol-4-yl)spiro[chroman-2,4′-piperidin]-4-one (150 mg, 0.329 mmol), [4-(methoxycarbonyl)phenyl]boronic acid (119 mg, 0.659 mmol), Cu(OAc)2 (90 mg, 0.494 mmol) in CH2Cl2 (1.5 ml) and the mixture was stirred at room temperature overnight. The mixture was filtered and the solvent was evaporated under reduced pressure. The residue was purified by silicagel column chromatography (hexane/EtOAc) to give intended compound as colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524730B2
出典データセットuspto-grants-2013_09
ORD IDord-237c1c2aa4ad44cba971796595c3eaf1
出典メモuspto-grants-2013_09