戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1874351作成日:2026年10月25日

Tert-butyl {4-methyl-3-[(6-nitropyridin-3-yl)oxy]phenyl}carbamate → Tert-butyl {3-[(6-aminopyridin-3-yl)oxy]-4-methylphenyl}carbamate

https://huagongshe.com/reaction/1874351

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-butyl {4-methyl-3-[(6-nitropyridin-3-yl)oxy]phenyl}carbamateHCID 57749145—
触媒HCID 178418390HCID 178418390—
溶媒MethanolHCID 887—
生成物Tert-butyl {3-[(6-aminopyridin-3-yl)oxy]-4-methylphenyl}carbamateHCID 57749176100.2%

反応手順

To a solution of tert-butyl {4-methyl-3-[(6-nitropyridin-3-yl)oxy]phenyl}carbamate (1.85 g, 5.35 mmol) in methanol (10 mL) was added palladium carbon (50% water-containing product, 100 mg), and the mixture was stirred under a hydrogen atmosphere at room temperature for 3 hr. The reaction mixture was filtered through celite, and the filtrate was concentrated under reduced pressure. The residue was dried to give the title compound (1.69 g, 99%) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08304557B2
出典データセットuspto-grants-2012_11
ORD IDord-89c2c9f2d1064e0ba002e1d4ee520fb1
出典メモuspto-grants-2012_11