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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-(2-Ethoxy-4-nitrophenyl)piperidin-2-one → HCID 59586675, 화합물

HRID 218531
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인쇄 미리보기

반응식

HRID 218531 반응식
[CH2:1]([O:3][C:4]1[CH:9]=[C:8]([N+:10]([O-])=O)[CH:7]=[CH:6][C:5]=1[N:13]1[CH2:18][CH2:17][CH2:16][CH2:15][C:14]1=[O:19])[CH3:2].[H][H]>C1COCC1.[Pd]>[NH2:10][C:8]1[CH:7]=[CH:6][C:5]([N:13]2[CH2:18][CH2:17][CH2:16][CH2:15][C:14]2=[O:19])=[C:4]([O:3][CH2:1][CH3:2])[CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 595867261-(2-Ethoxy-4-nitrophenyl)piperidin-2-oneHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 59586675HCID 59586675, 화합물

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8028Tetrahydrofuran용매

실험 절차

235 mg (0.889 mmol) of the product from example 90A are dissolved in 40 ml of THF and admixed with 50 mg of 10% palladium on activated carbon. Hydrogenation is effected in a hydrogen atmosphere under standard pressure overnight, then the mixture is filtered with suction through kieselguhr, washed three times with THF and concentrated cautiously under reduced pressure. This affords 262 mg of crude product, which is converted further without purification.

후처리

  1. filtrationthe mixture is filtered with suction through kieselguhr
  2. washwashed three times with THF
  3. concentrationconcentrated cautiously under reduced pressure
  4. customThis affords 262 mg of crude product, which is converted further without purification

출처 및 근거

ORD 기록
ord-47053602dd5a418fa447d7183d4fb3fd
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08198267B2

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