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HRID 971534作成日:2026年10月26日

Isoamyl Nitrite → HCID 178516177、化合物

https://huagongshe.com/reaction/971534

反応式

関与物質

役割名称HCID仕込み量
反応物Isoamyl NitriteHCID 8053—
反応物TriethylamineHCID 8471—
反応物L-Tryptophan benzyl esterHCID 7016092—
反応物HCID 178511799HCID 178511799—
溶媒Hydrochloric AcidHCID 313—
溶媒Dimethyl SulfoxideHCID 679—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 178516177HCID 178516177—

反応条件

温度-20 °C

反応手順

N-(5-Oxo-L-prolyl)-L-histidine hydrazide (0.840 g, 3 mmol) is dissolved in a solution at 0° C. of dry dimethylformamide (14 ml), dry dimethyl sulfoxide (10.5 ml) and 2.4 N anhydrous gaseous hydrogen chloride in dry tetrahydrofuran (7.5 ml). The solution is cooled to -20° C. and isoamyl nitrite (0.57 ml) is added with stirring. The solution is stirred for 30 minutes at -20° C. and is then cooled to -24° C. Triethylamine (3.2 ml) is slowly added until the solution is slightly alkaline pH 8-9. While stirring at -20° C., a solution of L-tryptophan benzyl ester (0.970 g, 3.3 mmol) in dry dimethylformamide (3.0 ml) is added. The solution is stirred at -20° C. for 30 minutes, at 0° C. for 30 minutes, and then at ice bath temperature for 18 hours. The solution is filtered and the precipitate is washed with dry dimethylformamide (2 × 2 ml). The combined filtrates are concentrated under reduced pressure at 40° C. The residue is dissolved in methanol (10 ml), diethyl ether (300 ml) is slowly added, and the precipitate is collected by filtration. The precipitate is once more dissolved in methanol (10 ml) and is precipitated by the addition of diethyl ether (300 ml). The precipitate is crystallized from methanol to give the title compound as a fine white powder, m.p. 250°-252° C., [α]D25 + 1.6° (c= 1.0, DMF).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04159980
出典データセットuspto-grants-1979_07
ORD IDord-1f0820bdc47e4958a31922296f662b0a
出典メモuspto-grants-1979_07