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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Piperazine → 4-Piperazin-1-yl-1-benzofuran-2-carboxamide

HRID 217
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HRID 217 반응식
C1CNCCN1.NC(=O)c1cc2c(Br)cccc2o1>C1CCOC1.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>NC(=O)c1cc2c(N3CCNCC3)cccc2o1
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참가 물질

7

반응물 2

HCID 4837PiperazineHCID 1125205634-Bromo-1-benzofuran-2-carboxamide

생성물 1

HCID 111959394-Piperazin-1-yl-1-benzofuran-2-carboxamide수율 0%

시약·촉매·용매 4

HCID 10796Cesium carbonate시약HCID 634876Binap, (A+-)-촉매
HCID 9811564
Bis(dibenzylideneacetone)palladium
촉매
HCID 8028Tetrahydrofuran용매

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온도
70 °C

실험 절차

The crude product from EN03731-54-001, 4-bromobenzofuran-2-carboxamide (0.600 g, 2.5 mmol), was dissolved in THF (18 mL) and water (18.00 mL). To this mixture were added piperazine (1.077 g, 12.50 mmol), Cesium carbonate (1.629 g, 5.00 mmol), Tris(dibenzylideneacetone)dipalladium(0) (0.114 g, 0.13 mmol) and rac-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl (0.156 g, 0.25 mmol) and the reaction was heated at 70 °C over night. 2010-04-13 No product was detected. The reaction mixture was filtered and solvents were removed in vacuo. The residue was partitioned between methylene chloride and water. The organic layer was washed with 1M HCl(aq), dired with sodium sulfate, filtered, concentrated and purified by flash chromatography(Isolute Si 70g, methylene chloride: methanol; 97:3). No product could be detected/isolated.

출처 및 근거

ORD 기록
ord-dc56e46e611f4db1889616d29baeeb5f
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
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