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HRID 562673作成日:2026年10月25日

tert-Butyl (5-nitropyridin-2-yl)carbamate → tert-butyl N-(5-aminopyridin-2-yl)carbamate

https://huagongshe.com/reaction/562673

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl (5-nitropyridin-2-yl)carbamateHCID 11064480—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
溶媒Ethyl AcetateHCID 8857—
生成物tert-butyl N-(5-aminopyridin-2-yl)carbamateHCID 2206444097%

反応手順

To a suspension of (tert-butoxy)-N-(5-nitro(2-pyridyl))carboxamide (0.27 g, 1.13 mmol) in methanol (2 mL), ethyl acetate (4 mL) and TEA (0.16 mL) was added 10% Pd/C (60 mg, 0.056 mmol) under argon. The reaction mixture was hydrogenated under 1 atm H2 for 20 hr, filtered through Celite and concentrated in vacuo to give N-(5-amino(2-pyridyl))(tert-butoxy)carboxamide (0.226 g, 97%). 1H-NMR. (DMSO-d6): δ 1.40 (s, 9H), 4.92 (br s, 2H), 6.89-6.91 (dd, 1H), 7.35-7.37 (d, 1H), 7.58 (d, 1H), 9.06 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08067428B2
出典データセットuspto-grants-2011_11
ORD IDord-10616adeecb24e31ae6c72226c405a61
出典メモuspto-grants-2011_11