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HRID 6367作成日:2026年10月24日

Hydrochloric Acid → 2-[[[5-(Dimethylamino)-1-naphthalenyl]sulfonyl]amino]-5-[[(phenylmethoxy)carbonyl]amino]pentanoic acid

https://huagongshe.com/ja/reaction/6367

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Dansyl chlorideHCID 11801—
反応物H-Orn(Z)-OHHCID 7009570—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium HydroxideHCID 14798—
生成物2-[[[5-(Dimethylamino)-1-naphthalenyl]sulfonyl]amino]-5-[[(phenylmethoxy)carbonyl]amino]pentanoic acidHCID 19793149—

反応条件

温度0 °C

反応手順

Nδ -Carbobenzyloxy-L-ornithine (39.6 g, 0.149 mol) was dissolved in a solution of 2N NaOH (90 mL) and tetrahydrofuran (200 mL) under nitrogen. After about 15 minutes at ambient temperature, the mixture was cooled to about 0° C. and subsequently treated with additional 2N NaOH (85 mL) and dansyl chloride (45.0 g, 0.167 mol) in 5 g portions over 15 minutes. The mixture was stirred at about 0° C. for about 1 hour and at room temperature for about 2 hours before it was neutralized to pH 7 with 1N HCl. The precipitate was suction-filtered and the filtrate was diluted with ethyl acetate. The organic phase was then separated, washed with brine, dried over Na2SO4 and concentrated to give a combined yield of 103.17 g (70.4%, two runs) of 2d as a yellow foam which was used directly.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05248673
出典データセットuspto-grants-1993_09
ORD IDord-d66b4eef54b0430690c4005529ed7d6e
出典メモuspto-grants-1993_09