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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23761생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/23761

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물N-HydroxyacetamidineHCID 30926—
반응물Boc-L-ValineHCID 83693—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물(S)-5-(1-amino-2-methylpropyl)-3-methyl-1,2,4-oxadiazoleHCID 29550895—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852745B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-63c05ebf483642babd18bb6d0f623481
출처 메모uspto-grants-2005_02