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Potassium Carbonate → 3-[1-(4-Pyridinylmethyl)-2-pyrrolidinyl]phenyl methylcarbamate

HRID 742562
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HRID 742562 반응식
[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][N:8]2[CH2:12][CH2:11][CH2:10][CH:9]2[C:13]2[CH:14]=[C:15]([OH:19])[CH:16]=[CH:17][CH:18]=2)=[CH:3][CH:2]=1.C(=O)([O-])[O-].[K+].[K+].[CH3:26][N:27]=[C:28]=[O:29]>O1CCCC1>[CH3:26][NH:27][C:28](=[O:29])[O:19][C:15]1[CH:16]=[CH:17][CH:18]=[C:13]([CH:9]2[CH2:10][CH2:11][CH2:12][N:8]2[CH2:7][C:4]2[CH:5]=[CH:6][N:1]=[CH:2][CH:3]=2)[CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 12228Methyl IsocyanateHCID 152932263-[1-(4-Pyridinylmethyl)-2-pyrrolidinyl]phenol

생성물 1

HCID 99048253-[1-(4-Pyridinylmethyl)-2-pyrrolidinyl]phenyl methylcarbamate수율 86%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a stirred solution of 3-[1-(4-pyridinylmethyl)-2-pyrrolidinyl]phenol (0.60 g) in dry tetrahydrofuran (16 ml) was added milled potassium carbonate (0.36 g), followed by methyl isocyanate (0.15 ml), dropwise, at ambient temperature, under nitrogen, with stirring. The mixture was stirred for 17 hrs and filtered through a pad of celite. The filter cake was washed with ethyl acetate, and the filtrate was concentrated. The residue was purified by flash column chromatography (silica gel, ether). The appropriate fractions were collected and concentrated to afford 0.63 g (86%) of product. Trituration of the residue with petroleum ether gave the analytical sample, mp 92°-105° C.

후처리

  1. stirringThe mixture was stirred for 17 hrs
  2. filtrationfiltered through a pad of celite
  3. washThe filter cake was washed with ethyl acetate
  4. concentrationthe filtrate was concentrated
  5. customThe residue was purified by flash column chromatography (silica gel, ether)
  6. customThe appropriate fractions were collected
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-4c7a7ec30c4b4ad188c6d4d9d86ec562
출처 데이터셋
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05554750

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