Potassium Carbonate → 5-(1,4,5,6-Tetrahydropyrimidin-1-yl)-3-methyl-2-nitro aniline

HRID 1354632ノート

反応式

HRID 1354632 の反応式
F[C:2]1[CH:3]=[C:4]([CH3:12])[C:5]([N+:9]([O-:11])=[O:10])=[C:6]([CH:8]=1)[NH2:7].[NH:13]1[CH2:18][CH2:17][CH2:16][N:15]=[CH:14]1.C(=O)([O-])[O-].[K+].[K+]>CS(C)=O.O>[N:15]1([C:2]2[CH:3]=[C:4]([CH3:12])[C:5]([N+:9]([O-:11])=[O:10])=[C:6]([CH:8]=2)[NH2:7])[CH2:16][CH2:17][CH2:18][N:13]=[CH:14]1

参加物

6

反応物 3

HCID 11430Potassium CarbonateHCID 1371051,4,5,6-TetrahydropyrimidineHCID 220210255-Fluoro-3-methyl-2-nitroaniline

生成物 1

HCID 235418765-(1,4,5,6-Tetrahydropyrimidin-1-yl)-3-methyl-2-nitro aniline収率 67.2%

試薬・触媒・溶媒 2

HCID 679Dimethyl Sulfoxide溶媒HCID 962Water溶媒

反応条件

温度
100 °C

実験手順

To a stirred solution of 2.0 g (11.76 mmol) of the 5-Flouro-3-methyl-2-nitro aniline in 10 mL of DMSO was added 1.2 g (14.11 mmol) of 1,4,5,6-Tetrahydropyrimidine, and 2.43 g (17.64 mmol) of potassium carbonate, and the mixture was heated at 100° C. for 10 hrs, cooled, diluted with water, and extracted with Ethylacetate containing 5% methanol. The combined organic extract was washed with water, brine and dried (Na2SO4). Evaporation of the solvent furnished the residue, which was chromatographed (20% of 2M ammonia in methanol and dichloromethane) to produce 1.85 g (67%) of the product as red solid. 1H NMR (400 MHz, CD3OD) δ 7.89 (1H, s), 6.53 (1H, d, J=2.57 Hz), 6.44 ((1H,d, J=2.1 Hz), 7.04 (1H, d, J=2.1 Hz), 3.70 (2H, t, J=6.0 Hz), 3.41 (2H, t, J=5.65 Hz, 2.43 (3H, s), 2.05 (2H, m) LCMS (M+H)+ m/z 235 (t=0.78 min).

後処理

  1. temperaturecooled
  2. extractionextracted with Ethylacetate containing 5% methanol
  3. extractionThe combined organic extract
  4. washwas washed with water, brine
  5. dry with materialdried (Na2SO4)
  6. customEvaporation of the solvent
  7. customfurnished the residue, which
  8. customwas chromatographed (20% of 2M ammonia in methanol and dichloromethane)

出典と根拠

ORDレコード
ord-1c5abd24cc8245239269d5af173e1a50
出典データセット
uspto-grants-2007_05
特許番号
US07223757B2

反応ノート

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