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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-(N-Boc-amino)piperidine → HCID 178418218, 화합물

HRID 63
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HRID 63 반응식
CC(C)(C)OC(=O)NC1CCNCC1.Clc1ccc2nccc(Cl)c2c1>CC(=O)N(C)C.CC(=O)O.CC(=O)O.CC1(C)c2cccc(P(c3ccccc3)c3ccccc3)c2Oc2c(P(c3ccccc3)c3ccccc3)cccc21.O=C([O-])[O-].[Cs+].[Cs+].[Pd]>NC1CCN(c2ccnc3ccc(Cl)cc23)CC1
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참가 물질

7

반응물 2

HCID 7238334-(N-Boc-amino)piperidineHCID 9360754,6-Dichloroquinoline

생성물 1

HCID 178418218HCID 178418218, 화합물수율 5%

시약·촉매·용매 4

HCID 10796Cesium carbonate시약HCID 6360441,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)촉매HCID 4144353Palladium (II) acetate촉매

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온도
150 °C

실험 절차

diacetoxypalladium (5.60 mg, 0.02 mmol) was added in one portion to tert-butyl piperidin-4-ylcarbamate (100 mg, 0.50 mmol), 4,6-dichloroquinoline (89 mg, 0.45 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (28.9 mg, 0.05 mmol) and cesium carbonate (488 mg, 1.50 mmol) in DMA (5 mL). The resulting mixture was stirred at 150 °C for 1 hour. LCMS analysis showed formation of a small amount of the desired product. The mixture was heated for a further 2 hours, after which time LCMS analysis showed loss of this small peak. Abandoned.

출처 및 근거

ORD 기록
ord-af3871564adb47f28d81d03aed7b6196
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
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HCID 31374
Dimethylacetamide
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