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HRID 1606907作成日:2026年10月27日

Triethylamine → 1-Amino-2-chloro-5a,6,7,8,9,9a-hexahydrodibenzofuran

https://huagongshe.com/reaction/1606907

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ethyl chloroformateHCID 10928—
反応物Tetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
反応物1-Amino-2-chloro-5a,6,7,8,9,9a-hexahydrodibenzofuran-4-carboxylic acidHCID 15136048—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
生成物1-Amino-2-chloro-5a,6,7,8,9,9a-hexahydrodibenzofuranHCID 19794430—

反応手順

To a cold solution of 0.3 g 1-amino-2-chloro-5a,6,7,8,9,9a-hexahydrodibenzofuran-4-carboxylic acid in 40 ml chloroform is added 0.3 g of triethylamine and then 0.2 g ethylchloroformate in 10 ml chloroform. Stirring is continued for 2 hours. This is then added to a cold mixture of 3 g 3-aminoguinuclidine dihydrochloride in 20 ml water containing 7.5 g K2CO3. Stirring is continued overnight. The reaction mxiture is then diluted with chloroform, the two layers separated and the chloroform layer washed twice with water, dried over magnesium sulfate and evaporated to dryness to give 1-amino-2-chloro-5a,6,7,8,9,9a-hexahydrodibenzo-furan-4-(N-1-azabicylo[2.2.2.]oct-3-yl]carboxamide as an oily product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04863921
出典データセットuspto-grants-1989_09
ORD IDord-7251e88d4d1c49b1a3b98f1aad464a24
出典メモuspto-grants-1989_09