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HRID 375438作成日:2026年10月24日

Triethylamine → HCID 56978006、化合物

https://huagongshe.com/ja/reaction/375438

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3-Indoleglyoxylyl chlorideHCID 89952—
反応物(3aS,4S,7aS)-7,7-diphenyl-4-(2-methoxyphenyl)perhydroisoindol-4-ol hydrochlorideHCID 70218598—
溶媒DichloromethaneHCID 6344—
生成物HCID 56978006HCID 5697800697.3%

反応手順

A solution of 0.43 g of 2-(3-indolyl)-2-oxoacetyl chloride in 20 cm3 of dry dichloromethane and then a solution of 0.6 cm3 of triethylamine in 5 cm3 of dry dichloromethane are added in succession to a suspension of 0.96 g of (3aS,4S,7aS)-7,7-diphenyl-4-(2-methoxyphenyl)perhydroisoindol-4-ol hydrochloride in 25 cm3 of dry dichloromethane at room temperature, while stirring. The reaction mixture is stirred at this temperature for 24 hours, subsequently diluted with 200 cm3 of dichloromethane, washed with 100 cm3 of an aqueous 1N solution of sodium hydroxide and with 50 cm3 of an aqueous saturated solution of sodium chloride, and is dried over magnesium sulphate and concentrated to dryness under reduced pressure (2.7 kPa). The residue is chromatographed on a Merck silica gel column (particle size 0.04-0.06 mm, diameter 2.5 cm, height 1 cm) by eluting under a pressure of 0.4 bar of nitrogen with a mixture of 1,2-dichloroethane and methanol (70/30 by volume) and collecting fractions of 15 cm3. Fractions 2 to 9 are combined and concentrated to dryness under reduced pressure (2.7 kPa). 1.15 g of (3aS,4S,7aS)-7,7-diphenyl-2-[2-oxo-2-(3-indolyl)acetyl]-4-(2-methoxyphenyl)perhydroisoindol-4-ol are obtained in the form of an orange foam.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05484804
出典データセットuspto-grants-1996_01
ORD IDord-06c4dca4b5eb4defb8c1dbf6a287d814
出典メモuspto-grants-1996_01