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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1468776생성일: 2026년 10월 27일

4-(4-Bromobenzyl)piperazine, N1-BOC protected → Tert-butyl 4-{4-[4-(1-methyl-6-oxo-1,6-dihydro-[4,4']bipyrimidinyl-2-yloxy)piperidin-1-yl]benzyl}piperazine-1-carboxylate

https://huagongshe.com/reaction/1468776

반응식

참여 물질

역할이름HCID투입량
반응물4-(4-Bromobenzyl)piperazine, N1-BOC protectedHCID 2795519—
반응물2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
반응물Sodium t-butoxideHCID 23676156—
반응물1-methyl-2-(piperidin-4-yloxy)-1H-[4,4']bipyrimidinyl-6-oneHCID 67977650—
촉매Palladium, tris[mu-[(1,2-eta:4,5-eta)-(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one]]di-, compd. with trichloromethane (1:1)HCID 11029508—
용매TolueneHCID 1140—
생성물Tert-butyl 4-{4-[4-(1-methyl-6-oxo-1,6-dihydro-[4,4']bipyrimidinyl-2-yloxy)piperidin-1-yl]benzyl}piperazine-1-carboxylateHCID 5093981140.4%

반응 조건

온도150 °C

반응 단계

To a mixture of tert-butyl 4-(4-bromo-benzyl)piperazine-1-carboxylate (371 mg, 1.04 mmol), 1-methyl-2-(piperidin-4-yloxy)-1H-[4,4′]bipyrimidinyl-6-one (300 mg, 1.04 mmol), tris(dibenzylideneacetone)dipalladium(0)-chloroform adduct (43.2 mg, 41.8 μmol) and 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (79.6 mg, 0.167 mmol) in toluene (2.09 ml) was added sodium tert-butoxide (151 mg, 1.57 mmol) under nitrogen atmosphere. The mixture was stirred at 150° C. for 30 minutes in Biotage Microwave reactor. The mixture was filtered through a pad of Celite, and concentrated in vacuo. The residue was purified by NH-silica gel column chromatography (eluent; hexane/ethyl acetate=1/1) to afford tert-butyl 4-{4-[4-(1-methyl-6-oxo-1,6-dihydro-[4,4′]bipyrimidinyl-2-yloxy)piperidin-1-yl]benzyl}piperazine-1-carboxylate as a pale yellow solid (236 mg, 0.420 mmol, 40%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09006232B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-5b00b3b7a9b3403c8c0b3c197f0e0f3b
출처 메모uspto-grants-2015_04