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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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tert-Butyl piperazine-1-carboxylate → HCID 178418197, 화합물

HRID 648
노트
인쇄 미리보기

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HRID 648 반응식
CC(C)(C)OC(=O)N1CCNCC1.CCOc1ccc(Br)cc1Cl>CC(=O)O.CC(=O)O.Cc1ccccc1.O=C([O-])[O-].[Cs+].[Cs+].[Pd].c1ccc(P(c2ccccc2)c2ccc3ccccc3c2-c2c(P(c3ccccc3)c3ccccc3)ccc3ccccc23)cc1>CCOc1ccc(N2CCN(C(=O)OC(C)(C)C)CC2)cc1Cl
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참가 물질

7

반응물 2

HCID 143452tert-Butyl piperazine-1-carboxylateHCID 219385134-Bromo-2-chloro-1-ethoxybenzene

생성물 1

HCID 178418197HCID 178418197, 화합물수율 0%

시약·촉매·용매 4

HCID 10796Cesium carbonate시약HCID 634876Binap, (A+-)-촉매HCID 4144353Palladium (II) acetate촉매

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온도
80 °C

실험 절차

In a 50 mL round-bottomed flask, PALLADIUM ACETATE (0.014 g, 0.06 mmol) was treated with BINAP (0.079 g, 0.13 mmol) under nitrogen in degassed Toluene (12.74 ml). The reaction was heated to 80 °C and was stirred for 10 min. To the flask was then added tert-butyl piperazine-1-carboxylate (0.237 g, 1.27 mmol), cesium carbonate (0.208 g, 0.64 mmol), potassium carbonate (0.176 g, 1.27 mmol), and 18-CROWN-6 (0.034 g, 0.13 mmol). The reaction was then treated with 4-bromo-2-chloro-1-ethoxybenzene (0.300 g, 1.27 mmol) and was allowed to stir at 80°C 5 h. **LCMS High pH:** No reaction observed

출처 및 근거

ORD 기록
ord-3dc45e0d006e4925b34d5e9919e16fc1
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
출처 보기

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이 페이지에서참가 물질반응 조건실험 절차출처 및 근거반응 노트
HCID 1140
Toluene
용매