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HRID 37337作成日:2026年10月24日

Sodium Hydroxide → (2S,4S)-4-(4-methoxybenzyl)thio-1-(4-nitrobenzyloxycarbonyl)-L-proline

https://huagongshe.com/ja/reaction/37337

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物4-Nitrobenzyl chloroformateHCID 78205—
反応物(4S)-4-{[(4-Methoxyphenyl)methyl]sulfanyl}-L-prolineHCID 15297070—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物(2S,4S)-4-(4-methoxybenzyl)thio-1-(4-nitrobenzyloxycarbonyl)-L-prolineHCID 1529707177.5%

反応手順

1.87 g of (2S,4S)-4-(4-methoxybenzylthio)-2-pyrrolidinecarboxylic acid [prepared as described in step (a) above] was suspended in 80 ml of a 1:1 by volume mixture of tetrahydrofuran and water. This suspension was then converted to a homogeneous solution by the addition of 7 ml of a 1N aqueous solution of sodium hydroxide. Whilst stirring this solution on an ice bath, 10 ml of a tetrahydrofuran solution containing 1510 mg of 4-nitrobenzyloxycarbonyl chloride and 7 ml of a 1N aqueous solution of sodium hydroxide were gradually added dropwise at the same time, and the resulting mixture was stirred under the same conditions for 10 minutes. At the end of this time, the tetrahydrofuran was removed by evaporation under reduced pressure. 1N aqueous hydrochloric acid was added to the reaction solution to adjust its pH to a value of between 2 and 3. The crystals which separated were collected by filtration, washed well with water and dried in the air. They were then further washed with a small amount of diethyl ether and dried, to obtain 2.42 g of the title compound, melting at 96°-98° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420119
出典データセットuspto-grants-1995_05
ORD IDord-95f2d28d048d4aed86abf3b0f36ff58c
出典メモuspto-grants-1995_05