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HRID 730832作成日:2026年10月26日

Diisopropylethylamine → Methyl N-{[(9H-fluoren-9-ylmethyl)oxy]carbonyl}-D-norleucylglycinate

https://huagongshe.com/reaction/730832

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Glycine methyl ester hydrochlorideHCID 122755—
反応物CarbodiimideHCID 160435—
反応物HOAtHCID 181649—
反応物(2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)hexanoic acidHCID 2756111—
溶媒DichloromethaneHCID 6344—
生成物Methyl N-{[(9H-fluoren-9-ylmethyl)oxy]carbonyl}-D-norleucylglycinateHCID 67401200—

反応手順

A mixture of fmoc-D-Nle-OH (10 g, 28.3 mmol, Novabiochem) and PS-carbodiimide (33 g, 42.45 mmol, 1.28 mmol/g, Argonaut Technologies Inc.) in dichloromethane (250 mL) was stirred at room temperature for 0.5 h. Then, glycine methyl ester hydrochloride (5.3 g, 42.45 mmol, Aldrich), HOAt (3.8 g, 28.3 mmol, Perseptive Biosystems) and diisopropylethylamine (16 mL, 84.9 mmol, Aldrich) were added and the mixture was stirred at room temperature for 16 h. The mixture was filtered and the resin was washed with dichloromethane (2×70 mL). The filtrate was concentrated in vacuo and the residue was purified by column chromatography, eluting with EtOAc/hexane (1:2) to give the title compound as a yellow solid. MS (ESI, positive ion) m/z: 425 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07582761B2
出典データセットuspto-grants-2009_09
ORD IDord-82221a597aeb4b0184ba9efcc11632d3
出典メモuspto-grants-2009_09