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Sodium Iodide → HCID 11952153, 화합물

HRID 251454
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HRID 251454 반응식
Cl[CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[O:13][CH2:14][C:15]([CH3:18])([CH3:17])[N:16]=2)=[CH:8][CH:7]=1.[I-].[Na+].[Na].[CH3:22][CH:23]1[CH2:27][CH2:26][CH:25]([CH3:28])[NH:24]1>C(#N)C.C(OCC)(=O)C.O>[CH3:22][CH:23]1[CH2:27][CH2:26][CH:25]([CH3:28])[N:24]1[CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[O:13][CH2:14][C:15]([CH3:18])([CH3:17])[N:16]=2)=[CH:8][CH:7]=1
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참가 물질

8

반응물 4

HCID 5238Sodium IodideHCID 960342,5-DimethylpyrrolidineHCID 5360545SodiumHCID 11950718HCID 11950718, 화합물

생성물 1

HCID 11952153HCID 11952153, 화합물수율 41%

시약·촉매·용매 3

HCID 962Water용매
HCID 6342
Acetonitrile
용매
HCID 8857Ethyl Acetate용매

실험 절차

2-[4-(3-chloropropoxy)phenyl]-4,4-dimethyl-4,5-dihydro-1,3-oxazole ax10 (500 mg, 1.87 mmol, 1 eq), sodium iodide (0.56 mg, 3.74 mmol, 2 eq), sodium hydrogenocarbonate (0.31 mg, 3.74 mmol, 2 eq) and 2,5-dimethylpyrrolidine (0.24 ml, 2.8 mmol, 1.5 eq) are stirred at reflux overnight in dry acetonitrile (10 ml). Water and ethyl acetate are added to the mixture and the layers are separated. The organic layer is dried with brine, sodium sulfate and evaporated under vacuum. Flash chromatography over silica with ethyl acetate as the eluent gives 0.253 g of 2-(4-{3-[2,5-dimethylpyrrolidin-1-yl]propoxy}phenyl)-4,4-dimethyl-4,5-dihydro-1,3-oxazole 18 as a free base.

후처리

  1. customthe layers are separated
  2. dry with materialThe organic layer is dried with brine, sodium sulfate
  3. customevaporated under vacuum

출처 및 근거

ORD 기록
ord-dcdf18bc8f604d12984beae1831bef3d
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07863450B2

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