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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 603228생성일: 2026년 10월 26일

Sulfuric acid magnesium salt (1:1) → 1-Benzyl 4-tert-butyl 2-[(4-{[(3,4-dichlorophenyl)amino]carbonyl}piperazin-1-yl)methyl]piperazine-1,4-dicarboxylate

https://huagongshe.com/reaction/603228

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric acid magnesium salt (1:1)HCID 24083—
반응물DiisopropylethylamineHCID 81531—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물N-(3,4-Dichlorophenyl)piperazine-1-carboxamideHCID 16775732—
반응물4-Boc-1-Cbz-piperazine-2-carbaldehydeHCID 59671527—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물1-Benzyl 4-tert-butyl 2-[(4-{[(3,4-dichlorophenyl)amino]carbonyl}piperazin-1-yl)methyl]piperazine-1,4-dicarboxylateHCID 57656842—

반응 단계

To 1-benzyl 4-tert-butyl 2-formylpiperazine-1,4-dicarboxylate (227 mg) in THF (20 ml) were added N-(3,4-dichlorophenyl)piperazine-1-carboxamide (179 mg), DIPEA (319 ul) DMF (1.6 ml) and MgSO4 (30 mg) the mixture stirred at room temperature for 30 minutes, sodium triacetoxyborohydride (277 mg) added and stirring continued for 16 hours at room temperature. Saturated aqueous sodium bicarbonate and ethyl acetate were added. The organic phase was dried (MgSO4) and evaporated to give the title compound as a semi-solid gum (331 mg, 84%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07906645B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-a7456215a8404e3184a2b6ecf57f4599
출처 메모uspto-grants-2011_03