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Carbon Tetrachloride → Methyl 2-[1-[(2,5-dimethylphenyl)acetyl]-4-piperidinyl]-4,5-dihydro-4-oxazolecarboxylate

HRID 2043732
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HRID 2043732 반응식
[CH3:1][O:2][C:3](=[O:27])[CH:4]([CH2:25]O)[NH:5][C:6]([CH:8]1[CH2:13][CH2:12][N:11]([C:14](=[O:24])[CH2:15][C:16]2[CH:21]=[C:20]([CH3:22])[CH:19]=[CH:18][C:17]=2[CH3:23])[CH2:10][CH2:9]1)=[O:7].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(N(CC)C(C)C)(C)C.C(Cl)(Cl)(Cl)Cl.C(=O)(O)[O-].[Na+]>C(#N)C.C(OCC)(=O)C.O.ClCCl>[CH3:23][C:17]1[CH:18]=[CH:19][C:20]([CH3:22])=[CH:21][C:16]=1[CH2:15][C:14]([N:11]1[CH2:10][CH2:9][CH:8]([C:6]2[O:7][CH2:25][CH:4]([C:3]([O:2][CH3:1])=[O:27])[N:5]=2)[CH2:13][CH2:12]1)=[O:24]
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참가 물질

10

반응물 5

HCID 5943Carbon TetrachlorideHCID 11776TriphenylphosphineHCID 81531DiisopropylethylamineHCID 516892Sodium BicarbonateHCID 67461522N-[[1-[(2,5-dimethylphenyl)acetyl]-4-piperidinyl]carbonyl]-DL-serine methyl ester2회

생성물 1

HCID 67460115
Methyl 2-[1-[(2,5-dimethylphenyl)acetyl]-4-piperidinyl]-4,5-dihydro-4-oxazolecarboxylate

시약·촉매·용매 4

HCID 962Water용매HCID 6342Acetonitrile용매HCID 6344Dichloromethane용매HCID 8857Ethyl Acetate용매

실험 절차

To a solution of N-[[1-[(2,5-dimethylphenyl)acetyl]-4-piperidinyl]carbonyl]-DL-serine methyl ester (i.e. the product of Example 9, Step C) (2.59 g, 6.88 mmol) in 25 mL of dry acetonitrile and 7 mL of dry dichloromethane was added triphenylphosphine (2.71 g, 10.32 mmol) and then N,N-diisopropylethylamine (1.6 g, 12.38 mmol). The reaction mixture was stirred until homogeneous, and carbon tetrachloride (1.59 g, 10.32 mmol) was added dropwise over 5 minutes. The reaction mixture was stirred for 2.5 h at room temperature, cooled to 0° C. and diluted with 50 mL of ethyl acetate followed by 15 mL of saturated aqueous sodium bicarbonate solution. The mixture was stirred for 10 minutes, poured into 40 mL of water, and the organic layer was separated, washed with brine, dried over MgSO4 and concentrated under reduced pressure to give 6 g of a yellow oil. The oil was purified by flash chromatography on silica gel using 50-100% of ethyl acetate in hexanes to give 900 mg of the title compound. 360 mg of starting amide was also recovered from the reaction mixture.

후처리

  1. additionwas added dropwise over 5 minutes
  2. temperaturecooled to 0° C.
  3. stirringThe mixture was stirred for 10 minutes
  4. customthe organic layer was separated
  5. washwashed with brine
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-10304786c2a14b3fb7ba27cdd6dee3dd
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08586611B2

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