戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 131656作成日:2026年10月27日

3-Heptanone → 2-(s)-(1-Propyl-butylamino)-pentanoic acid [5-(5-hydroxy-1,5-dimethyl-hexyl)-thiazol-2-yl]-amide

https://huagongshe.com/reaction/131656

反応式

関与物質

役割名称HCID仕込み量
反応物3-HeptanoneHCID 7802—
反応物Sodium SulfateHCID 24436—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物2-(S)-amino-pentanoic acid [5-(5-methoxy-1,5-dimethyl-hexyl)-thiazol-2-yl]-amide HCl saltHCID 131726918—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
溶媒1,1-DichloroethaneHCID 6365—
生成物2-(s)-(1-Propyl-butylamino)-pentanoic acid [5-(5-hydroxy-1,5-dimethyl-hexyl)-thiazol-2-yl]-amideHCID 11654783—

反応条件

温度40 °C

反応手順

A mixture of 2-(S)-amino-pentanoic acid [5-(5-methoxy-1,5-dimethyl-hexyl)-thiazol-2-yl]-amide HCl salt (100 mg, 0.265 mmol) and 3-heptanone (0.1 mL), acetic acid (0.2 mL), sodium sulfate and sodium cyanoborohydride (100 mg) in dichloroethane (2 mL) and methanol (1 mL) was stirred at 40° C. overnight. The mixture was quenched with water, basified by dilute sodium hydroxide, and extracted with methylene chloride. The organic layer was concentrated to dryness. The residue was purified by Biotage silica gel column chromatography to isolate 2-(S)-(1-propyl-butylamino)-pentanoic acid [5-(5-hydroxy-1,5-dimethyl-hexyl)-thiazol-2-yl]-amide as a colorless oil, LC-MS, RT=2.2 min, M+1=426.5.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07384968B2
出典データセットuspto-grants-2008_06
ORD IDord-59679df6d87c47658f1cf87b4a0d71bc
出典メモuspto-grants-2008_06