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HRID 1060699作成日:2026年10月27日

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

https://huagongshe.com/reaction/1060699

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US06525064B1
出典データセットuspto-grants-2003_02
ORD IDord-dd8b9dcba75d4ad4b01fad8f2f3e159f
出典メモuspto-grants-2003_02