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HCID 18327906, 화합물 → tert-Butyl 4-(pyrimidin-2-yl)piperidine-1-carboxylate

HRID 1250305
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HRID 1250305 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][C:11]([C:14]2[N:19]=[CH:18][CH:17]=[CH:16][N:15]=2)=[CH:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]>C(O)C.[C].[Pd]>[C:1]([O:5][C:6]([N:8]1[CH2:9][CH2:10][CH:11]([C:14]2[N:15]=[CH:16][CH:17]=[CH:18][N:19]=2)[CH2:12][CH2:13]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 18327906HCID 18327906, 화합물

생성물 1

HCID 18328041tert-Butyl 4-(pyrimidin-2-yl)piperidine-1-carboxylate수율 33%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 702Ethanol용매

실험 절차

490 mg of the compound of step 2 of Example 25 was dissolved in 10 ml of ethanol, 100 mg of 10% palladium carbon was added, then the resultant mixture was agitated under hydrogen gas for 2 days. The catalyst was filtered out, the ethanol was distilled off, and the residue was refined with silica gel column chromatography (hexane:ethyl acetate=1:1) to obtain the above-referenced compound in an amount of 160 mg (yield of 33%).

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후처리

  1. filtrationThe catalyst was filtered out
  2. distillationthe ethanol was distilled off
  3. customto obtain the above-referenced compound in an amount of 160 mg (yield of 33%)

출처 및 근거

ORD 기록
ord-ec1a51ba799b4658a82cef9cc3e308e6
출처 데이터셋
uspto-grants-2002_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06337397B1

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