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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2043728생성일: 2026년 10월 24일

4-Methylmorpholine → 1,1-dimethylethyl 4-[4-[[methyl[(1R)-1,2,3,4-tetrahydro-1-naphthalenyl]amino]carbonyl]-2-oxazolyl]-1-piperidinecarboxylate

https://huagongshe.com/ko/reaction/2043728

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물(R)-N-Methyl-1,2,3,4-tetrahydronaphthalen-1-amineHCID 7128544—
반응물2-{1-[(Tert-butoxy)carbonyl]piperidin-4-yl}-1,3-oxazole-4-carboxylic acidHCID 67461583—
용매DichloromethaneHCID 6344—
생성물1,1-dimethylethyl 4-[4-[[methyl[(1R)-1,2,3,4-tetrahydro-1-naphthalenyl]amino]carbonyl]-2-oxazolyl]-1-piperidinecarboxylateHCID 6746089340.5%

반응 단계

A mixture of 1-(1,1-dimethylethyl) 4-(4-carboxy-2-oxazolyl)-1-piperidinecarboxylate (600 mg, 2.02 mmol), 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (425.57 mg, 2.22 mmol) and N-methylmorpholine (224.55 mg, 2.22 mmol) in 4 mL dichloromethane was stirred for 15 minutes at room temperature. To the reaction mixture was added 424 mg (2.63 mmol) of (1R)-1,2,3,4-tetrahydro-N-methyl-1-naphthalenamine was added and the reaction mixture was stirred for 16 h. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel chromatography using 25-75% of ethyl acetate in hexanes as eluant to give 360 mg of the title compound as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08586611B2
출처 데이터셋uspto-grants-2013_11
ORD IDord-dda2aa44125b489d91f55899f0a50dbe
출처 메모uspto-grants-2013_11