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HRID 580385作成日:2026年10月26日

Iodoethane → HCID 15128680、化合物

https://huagongshe.com/reaction/580385

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物DiisopropylamineHCID 7912—
反応物Lithium diisopropylamideHCID 2724682—
反応物HCID 14156194HCID 14156194—
反応物Carbontetrachloride dry-iceHCID 86602444—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
溶媒HexamethylphosphoramideHCID 12679—
生成物HCID 15128680HCID 15128680—

反応条件

温度-78 °C

反応手順

To a freshly prepared solution of lithium diisopropylamide in tetrahydrofuran (6 equivalents; prepared by addition of 19.2 ml of a 2.6M solution of n-butyllithium in hexane to 15 ml of freshly distilled diisopropylamine in 80 ml of tetrahydrofuran) at -78° C., was added 3.0 g (8.35 mmole) of 7-chloro-1,3,4,5-tetrahydro-3-(methoxycarbonyl)-4-(4-methoxyphenyl)-2H-1-benzazepin-2-one (see Example 1C . After stirring at -78° C. for 1.5 hours, 3 ml of hexamethylphosphoric triamide was added along with 13.6 ml of iodoethane (filtered through alumina to remove iodine). The mixture was stirred at -78° C. for 30 minutes (under argon), and then at -20° C. (dry-ice/carbon tetrachloride bath) for six days. The reaction was quenched with 1N hydrochloric acid (50 ml), and the aqueous layer was extracted with ethyl acetate (three times). The ethyl acetate extracts and the tetrahydrofuran were combined, washed with saturated sodium bicarbonate and saturated sodium chloride, and dried (magnesium sulfate). The solution was concentrated, combined with 0.31 g of previously prepared crude product and flash chromatographed (silica gel/3:1-hexane:ethyl acetate) yielding 0.61 g of product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04752645
出典データセットuspto-grants-1988_06
ORD IDord-ef2f98eaa704433298f15a3ed1736cee
出典メモuspto-grants-1988_06