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Cyanuric chloride → Methyl 4-[(4,5-diisopropylfuran-2-carbonyl)amino]benzoate

HRID 1023704
ノート
印刷プレビュー

反応式

HRID 1023704 の反応式
[CH:1]([C:4]1[CH:5]=[C:6]([C:12]([OH:14])=O)[O:7][C:8]=1[CH:9]([CH3:11])[CH3:10])([CH3:3])[CH3:2].N1C(Cl)=NC(Cl)=NC=1Cl.C(N(CC)CC)C.[NH2:31][C:32]1[CH:41]=[CH:40][C:35]([C:36]([O:38][CH3:39])=[O:37])=[CH:34][CH:33]=1>CC(C)=O.CN(C)C1C=CN=CC=1>[CH:1]([C:4]1[CH:5]=[C:6]([C:12]([NH:31][C:32]2[CH:33]=[CH:34][C:35]([C:36]([O:38][CH3:39])=[O:37])=[CH:40][CH:41]=2)=[O:14])[O:7][C:8]=1[CH:9]([CH3:10])[CH3:11])([CH3:2])[CH3:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 7954Cyanuric chlorideHCID 8471TriethylamineHCID 12082Methyl 4-aminobenzoateHCID 584205144,5-Diisopropylfuran-2-carboxylic acid

生成物 1

HCID 67395533Methyl 4-[(4,5-diisopropylfuran-2-carbonyl)amino]benzoate収率 89.3%

試薬・触媒・溶媒 2

HCID 14284
4-(Dimethylamino)pyridine
触媒
HCID 180Acetone溶媒

実験手順

A solution of 4,5-diisopropylfuran-2-carboxylic acid (50 mg, 0.255 mmol) and cyanuric chloride (71 mg, 0.385 mmol) in acetone (3 ml) was added with triethylamine (142 μl, 1.021 mmol), and the mixture was stirred at room temperature for 3.5 hours. The reaction mixture was added with methyl 4-aminobenzoate (77 mg, 0.510 mmol), and the mixture was further stirred for 14 hours. The reaction solvent was evaporated, then the residue was dissolved in pyridine (1 ml), the solution was added with 4-dimethylaminopyridine (1 mg, 8.20 μmol), and the mixture was stirred at room temperature for 4 hours. Pyridine was evaporated, and then the reaction mixture was dissolved in 10% methanol-chloroform, the solution was added with silica gel (1.0 g), and the mixture was evaporated to dryness. The residue was purified by silica gel chromatography [hexane-ethyl acetate (6:1)] to obtain methyl 4-[(4,5-diisopropylfuran-2-carbonyl)amino]benzoate (75 mg, 89%) as colorless prisms.

後処理

  1. stirringthe mixture was further stirred for 14 hours
  2. customThe reaction solvent was evaporated
  3. dissolutionthe residue was dissolved in pyridine (1 ml)
  4. stirringthe mixture was stirred at room temperature for 4 hours
  5. customPyridine was evaporated
  6. dissolutionthe reaction mixture was dissolved in 10% methanol-chloroform
  7. additionthe solution was added with silica gel (1.0 g)
  8. customthe mixture was evaporated to dryness
  9. customThe residue was purified by silica gel chromatography [hexane-ethyl acetate (6:1)]

出典と根拠

ORDレコード
ord-a939961a1e2345c4ad57a37bd8d47e01
出典データセット
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08722730B2

反応ノート

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