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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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N-Butylnicotinamide → HCID 20298115, 화합물

HRID 1389162
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HRID 1389162 반응식
[CH2:1]([NH:5][C:6](=[O:13])[C:7]1[CH:12]=[CH:11][CH:10]=[N:9][CH:8]=1)[CH2:2][CH2:3][CH3:4]>C(O)(=O)C.[Pt]=O>[CH2:1]([NH:5][C:6]([CH:7]1[CH2:12][CH2:11][CH2:10][NH:9][CH2:8]1)=[O:13])[CH2:2][CH2:3][CH3:4]
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참가 물질

4

반응물 1

HCID 506608N-Butylnicotinamide

생성물 1

HCID 20298115HCID 20298115, 화합물수율 52.5%

시약·촉매·용매 2

HCID 82844Platinum oxide (PtO)촉매HCID 176Acetic Acid용매

실험 절차

N-n-Butylnicotinamide (7.0 g) in acetic acid (100 ml) was hydrogenated over platinum oxide at 50° and 50 p.s.i. The catalyst was removed by filtration, the filtrate evaporated and the residue treated with toluene and evaporated in vacuo. The residue in chloroform (50 ml) was washed with sodium bicarbonate solution (3×50 ml) the organic layer separated, dried (Na2SO4) and the solvent evaporated in vacuo to give as an oil 3-(N-n-butylcarbamoyl)piperidine (3.8 g).

후처리

  1. customThe catalyst was removed by filtration
  2. customthe filtrate evaporated
  3. additionthe residue treated with toluene
  4. customevaporated in vacuo
  5. washThe residue in chloroform (50 ml) was washed with sodium bicarbonate solution (3×50 ml) the organic layer
  6. customseparated
  7. dry with materialdried (Na2SO4)
  8. customthe solvent evaporated in vacuo

출처 및 근거

ORD 기록
ord-f3921004db8d40858362aff62f74763d
출처 데이터셋
uspto-grants-1981_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04243666

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