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HRID 2055652作成日:2026年10月26日

Methanol → Methyl 4-((tert-butoxycarbonyl)amino)nicotinate

https://huagongshe.com/reaction/2055652

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Potassium CarbonateHCID 11430—
反応物Sodium ThiosulfateHCID 24477—
反応物N-IodosuccinimideHCID 120273—
反応物tert-Butyl (3-formylpyridin-4-yl)carbamateHCID 819566—
生成物Methyl 4-((tert-butoxycarbonyl)amino)nicotinateHCID 2343872996%

反応手順

Formula 504 where R1, R3 and R4 are H; W. Y and Z are —C═; and X is —N═: To a solution of methanol (100 mL) and N-Boc-4-amino-3-pyridine carboxyaldehyde (8.3 g, 37.3 mmol), were added N-iodosuccinimide (21.0 g, 93.4 mmol) and potassium carbonate (12.9 g, 93.4 mmol) at room temperature. The mixture was stirred for 1 hour and then poured into a saturated Na2S2O3 solution (100 mL). After further dilution with water (100 mL) the mixture was extracted with dichloromethane (3×100 mL). The combined organic layers were dried over sodium sulfate and concentrated under reduced pressure to give the pure desired methyl ester product, 4-tert-butoxycarbonylamino-nicotinic acid methyl ester (9.0 g, 96%). MS (Cl) m/e: 253.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07332498B2
出典データセットuspto-grants-2008_02
ORD IDord-214cfd9a793247d3adb5cd2dbdbf3381
出典メモuspto-grants-2008_02