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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1446300생성일: 2026년 10월 27일

Diisopropylethylamine → 3-({1-[(5-Phenyl-1,3-oxazol-4-yl)carbonyl]pyrrolidin-2-yl}methyl)pyridine

https://huagongshe.com/reaction/1446300

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물5-Phenyl-1,3-oxazole-4-carboxylic acidHCID 2776299—
반응물3-(2-Pyrrolidinylmethyl)pyridineHCID 3263876—
용매DimethylformamideHCID 6228—
생성물3-({1-[(5-Phenyl-1,3-oxazol-4-yl)carbonyl]pyrrolidin-2-yl}methyl)pyridineHCID 59170172—

반응 단계

5-Phenyl-1,3-oxazole-4-carboxylic acid (40 mg, 0.211 mmol), 3-(pyrrolidin-2-ylmethyl)pyridine (50.5 mg, 0.215 mmol), O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (86.2 mg, 0.268 mmol) and diisopropylethylamine (25.4 mg, 0.197 mmol) were mixed in dimethylformamide (1.0 mL) and stirred at room temperature. Solvent was evaporated in vacuo, and the residue was taken up in methanol (1 mL), filtered and purified by preparative chromatography. The combined fractions were partitioned between NaHCO3 (sat) and ethylacetate. The organic layer was washed with water and concentrated in vacuo to afford the title compound. HRMS (ESI, pos. ion) m/z calcd for C20H19N3O2: 333.1477, found 333.1484.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07666888B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-38be1efd17b849f497a1609bfaf62c92
출처 메모uspto-grants-2010_02