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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Piperidine → 2-Fluoro-4-piperidin-1-ylbenzonitrile

HRID 110
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HRID 110 반응식
C1CCNCC1.N#Cc1ccc(Br)cc1F>CC(=O)O.CC(=O)O.CC(C)(C)[O-].CC(C)c1cc(C(C)C)c(-c2ccccc2P(C2CCCCC2)C2CCCCC2)c(C(C)C)c1.Cc1ccccc1.[Na+].[Pd]>N#Cc1ccc(N2CCCCC2)cc1F
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참가 물질

7

반응물 2

HCID 8082PiperidineHCID 7360294-Bromo-2-fluorobenzonitrile

생성물 1

HCID 794218452-Fluoro-4-piperidin-1-ylbenzonitrile수율 49.37%

시약·촉매·용매 4

HCID 23676156Sodium t-butoxide시약HCID 4144353Palladium (II) acetate촉매
HCID 11155794
2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl
촉매
HCID 1140Toluene용매

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온도
160 °C

실험 절차

4-bromo-2-fluorobenzonitrile (119 mg, 0.59 mmol), Piperidine (0.059 mL, 0.59 mmol), Palladium(II) acetate (6.68 mg, 0.03 mmol), dicyclohexyl(2',4',6'-triisopropylbiphenyl-2-yl)phosphine (14.18 mg, 0.03 mmol) and sodium tert-butoxide (57.2 mg, 0.59 mmol) were suspended in toluene (4 mL) and tBuOH (0.800 mL) and heated to 160°C for 10 minutes in the microwave. LCMS indicated incomplete reaction, thus, the reaction mixture was heated to 160°C for a further 20 minutes. Still incomplete reaction however, the reaction mixture was diluted with EtOAc (10 mL), and washed sequentially with water (10 mL), and saturated brine (10 mL). The organic layer was dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 100% EtOAc in isohexane. A yellow oil (60mg) was isolated but NMR revealed this not be the desired product. No further work done.

출처 및 근거

ORD 기록
ord-2e557d69002c4320a9c5c7d56e530a90
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
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