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HRID 2164297作成日:2026年10月25日

Triethylamine → 7-(2-Fluorobenzoyl)-3-(methylsulfanyl)-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/2164297

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-Amino-2'-fluorobenzophenoneHCID 74101—
反応物Tert-Butyl hypochloriteHCID 521297—
反応物Ethyl methylthioacetateHCID 12284386—
溶媒DichloromethaneHCID 6344—
生成物7-(2-Fluorobenzoyl)-3-(methylsulfanyl)-1,3-dihydro-2H-indol-2-oneHCID 1339428355%

反応手順

A solution of 86 g (0.4 mole) of 2-amino-2'-fluorobenzophenone in 3 liters of methylene chloride was cooled to -65° C. and 54 g (0.4 mole) of ethyl methylthioacetate was added. A solution of 46 g (0.42 mole) of 95% tertiary butoxy chloride in 100 ml of methylene chloride was added dropwise, keeping the temperature below -65° C. One hour after addition was complete, 41 g (0.4 mole) of triethylamine was added dropwise and the mixture allowed to warm to room temperature. The solution was concentrated to about 1400 ml and then washed with water. The organic solution was concentrated and the residue dissolved in 800 ml methanol containing 60 ml of concentrated hydrochloric acid. The mixture was heated at reflux for one hour followed by cooling. The mixture stood overnight, then the crystals were collected and recrystallized from 20% aqueous ethanol to give 66 g (55%)pale yellow needles; m.p. 147.0°-148.5° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04503073
出典データセットuspto-grants-1985_03
ORD IDord-ed0c19579f994703af3753e6ad4658b9
出典メモuspto-grants-1985_03