Acetic Acid → Ethyl 2,4-dimethyl-6-oxo-1-phenyl-1,6-dihydropyridine-3-carboxylate

HRID 222789

反応式

HRID 222789 の反応式
[CH2:1]([O:3][C:4]([C:6]1[C:7]([CH3:14])=[CH:8][C:9](=[O:13])O[C:11]=1[CH3:12])=[O:5])[CH3:2].[NH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.C(O)(=O)C.C(NC1C=CC=CC=1)(=O)C.C(NC1C=CC(C(=O)C)=CC=1)(=O)C>>[CH2:1]([O:3][C:4]([C:6]1[C:7]([CH3:14])=[CH:8][C:9](=[O:13])[N:15]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[C:11]=1[CH3:12])=[O:5])[CH3:2]

参加物

6

反応物 5

HCID 176Acetic AcidHCID 904AcetanilideHCID 6115AnilineHCID 75937N-(p-acetylphenyl)acetamideHCID 76918ethyl 4,6-dimethyl-2-oxo-2H-pyran-5-carboxylate

生成物 1

HCID 11651942Ethyl 2,4-dimethyl-6-oxo-1-phenyl-1,6-dihydropyridine-3-carboxylate収率 32.6%

実験手順

A mixture of 4,6-dimethyl-2-oxo-2H-pyran-5-carboxylic acid ethyl ester (=ethyl isodehydroacetate, 1.967 g, 10.02 mmol), aniline (1.865 g, 20.03 mmol) and acetic acid (0.5 mL, 9 mmol) was shaken at 90 C for 5 hours, then at 55° C. for 3 days. The excess of volatiles were removed in vacuo (0.1 mbar, 70 C, 30 min). It was transferred on to a SiO2 column (50 g) with 1,2-dichloroethane/heptane 1:3 purified by flash chromatography with gradient 20% to 100% of ethyl acetate in heptane. The pure fractions gave 906 mg of the title compound as pale yellow oil, yield 33% (non-pure additional fractions gave 886 mg of the title compound contaminated with acetanilide and 4′-acetamidoacetophenone). LC-MS (m/z) 272.4 (MH+); tR=1.07. 1H NMR (600 MHz, DMSO-d6): 1.28 (t, J=7.1 Hz, 3H, Me of Et), 1.9 (s, 3H, 2-Me), 2.16 (d, J=0.9 Hz, 3H, 4-Me), 4.28 (q, J=7.1 Hz, 2H, CH2 of Et), 6.3 (s, 1H, 5-H), 7.27 (dm, J=7.7 Hz, J<1.5 Hz, 2H, two ortho-H of Ph), 7.47 (tt, J=7.4 Hz, J=1.2 Hz, 1H, para-H of Ph), 7.53 (tm, J=7.5 Hz, J<1.7 Hz, 2H, two meta-H of Ph).

後処理

  1. waitat 55° C. for 3 days
  2. customThe excess of volatiles were removed in vacuo (0.1 mbar, 70 C, 30 min)
  3. custompurified by flash chromatography with gradient 20% to 100% of ethyl acetate in heptane
  4. customThe pure fractions gave

出典と根拠

ORDレコード
ord-c2ae4e2c9a1f4d3fbe419b6dd011b6a7
出典データセット
uspto-grants-2012_06
特許番号
US08207347B2

関連ノート

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