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HRID 1647015作成日:2026年10月26日

Pyridine → Isopropyl 1-amino-4-bromoanthraquinone-2-carboxylate

https://huagongshe.com/reaction/1647015

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物1,2-DichlorobenzeneHCID 7239—
反応物Thionyl ChlorideHCID 24386—
反応物1-Amino-4-bromo-9,10-dioxo-9,10-dihydroanthracene-2-carboxylic acidHCID 271593—
溶媒TolueneHCID 1140—
溶媒O-XyleneHCID 7237—
溶媒ChlorobenzeneHCID 7964—
生成物Isopropyl 1-amino-4-bromoanthraquinone-2-carboxylateHCID 19800488—

反応手順

The starting 1-amino-4-bromoanthraquinone-2-carboxylic acid is reacted with 1.5 to 3 molar equivalents of a chlorinating agent such as thionyl chloride at a temperature of 80° to 100° C. for a period of about 1 to 3 hours in the presence of 0.01 to 5 molar equivalents (based on the raw material) of pyridine in 3 to 7-fold weight a amount of an inert solvent such as orthodichlorobenzene, chlorobenzene, toluene or xylene so as to be converted into an acid chloride. After the excess chlorinating agent has been removed therefrom under reduced pressure, 1.5 to 5 molar equivalents of isopropyl alcohol is added thereto and esterification is then performed at 60° to 80° C. for 1 to 3 hours. Afterward, the product is allowed to stand, thereby obtaining crystals of isopropyl 1-amino-4-bromoanthraquinone-2-carboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05182395
出典データセットuspto-grants-1993_01
ORD IDord-6794cf50d8644b1f9d0bd07864d3b5a3
出典メモuspto-grants-1993_01