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1,4-Dibromobenzene → Methyl 2-(4-(4-bromophenyl)piperazin-1-yl)acetate

HRID 475
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HRID 475 반응식
Brc1ccc(Br)cc1.COC(=O)CN1CCNCC1>C1COCCO1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C([O-])[O-].[Cs+].[Cs+].[Pd].[Pd].c1ccc(P(c2ccccc2)c2ccc3ccccc3c2-c2c(P(c3ccccc3)c3ccccc3)ccc3ccccc23)cc1>COC(=O)CN1CCN(c2ccc(Br)cc2)CC1
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참가 물질

7

반응물 2

HCID 78041,4-DibromobenzeneHCID 153431581-Piperazineacetic acid, methyl ester

생성물 1

HCID 58064520Methyl 2-(4-(4-bromophenyl)piperazin-1-yl)acetate수율 0%

시약·촉매·용매 4

HCID 10796Cesium carbonate시약HCID 634876Binap, (A+-)-촉매
이 페이지에서참가 물질반응 조건실험 절차출처 및 근거반응 노트
HCID 9811564
Bis(dibenzylideneacetone)palladium
촉매
HCID 312751,4-Dioxane용매

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온도
85 °C

실험 절차

In a reaction vial, 1,4-dibromobenzene (0.373 g, 1.58 mmol), methyl 2-(piperazin-1-yl)acetate (0.100 g, 0.63 mmol), CS2CO3 (0.309 g, 0.95 mmol), and BINAP (0.024 g, 0.04 mmol) were taken up in 1,4-dioxane (1.5 ml). Argon was bubbled through the solution for 1 minute. Pd2(dba)3 (0.012 g, 0.01 mmol) was added, followed by additional purging with argon. The vial was capped and placed on the heater-shaker. The reaction was stirred (450 rpm) at 100 °C overnight. LC/MS at this point did not indicate any formation of the dp. Experiment not progressed.

출처 및 근거

ORD 기록
ord-cf737b8f3d9340aca6130b04f75e7c21
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
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