戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 11368作成日:2026年10月24日

Toluene → tert-butyl 2-(2,6,7-trimethyl-4-phenoxy-1H-imidazo[4,5-c]pyridin-1-yl)ethylcarbamate

https://huagongshe.com/ja/reaction/11368

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Triethyl orthoacetateHCID 66221—
反応物Pyridinium chlorideHCID 10176127—
反応物Tert-butyl 2-[(3-amino-5,6-dimethyl-2-phenoxypyridin-4-yl)amino]ethylcarbamateHCID 21973843—
溶媒Ethyl AcetateHCID 8857—
生成物tert-butyl 2-(2,6,7-trimethyl-4-phenoxy-1H-imidazo[4,5-c]pyridin-1-yl)ethylcarbamateHCID 21973834100%

反応手順

A mixture of tert-butyl 2-[(3-amino-5,6-dimethyl-2-phenoxypyridin-4-yl)amino]ethylcarbamate (43.7 g, 117 mmol), triethyl orthoacetate (22.6 mL, 123 mmol), pyridine hydrochloride (4.4 g) and toluene (440 mL) was heated at reflux for 30 minutes. The reaction mixture was concentrated under reduced pressure to provide a brown oil. The oil was dissolved in ethyl acetate (1 L) and washed with water (2×500 mL). The aqueous washes were combined and extracted with ethyl acetate (2×500 mL). The combined organics were washed with brine, dried over magnesium sulfate and then concentrated under reduced pressure to provide 46.4 g of tert-butyl 2-(2,6,7-trimethyl-4-phenoxy-1H-imidazo[4,5-c]pyridin-1-yl)ethylcarbamate as a white solid, m.p. 180–182° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098221B2
出典データセットuspto-grants-2006_08
ORD IDord-b26a23f2ad984f5d9be603e103503082
出典メモuspto-grants-2006_08