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HRID 23761作成日:2026年10月26日

Dicyclohexylcarbodiimide → (S)-5-(1-amino-2-methylpropyl)-3-methyl-1,2,4-oxadiazole

https://huagongshe.com/reaction/23761

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物N-HydroxyacetamidineHCID 30926—
反応物Boc-L-ValineHCID 83693—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
生成物(S)-5-(1-amino-2-methylpropyl)-3-methyl-1,2,4-oxadiazoleHCID 29550895—

反応手順

A solution of BOC-L-valine (4.34 g, 20.0 mmol) in dichloromethane (20 mL) was cooled to 0° C. and treated dropwise with a solution of dicyclohexylcarbodiimide (2.06 g, 10.0 mmol) in dichloromethane (5 mL). After 1 hour the white solid which had formed was removed by filtration and the filtrate concentrated under reduced pressure. The residue was dissolved in pyridine (15 mL) and treated with acetamidoxime (488 mg, 6.6 mmol) in pyridine (5 mL) and the mixture heated at reflux for 1 hour. The pyridine was evaporated under reduced pressure and the residue partitioned between ethyl acetate and water. The organic phase was washed several times with water, dried over magnesium sulfate and concentrated. The residue was chromatographed on silica gel using 10% ethyl acetate in hexanes to elute the product (0.62 g, 25%) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06852745B2
出典データセットuspto-grants-2005_02
ORD IDord-63c05ebf483642babd18bb6d0f623481
出典メモuspto-grants-2005_02