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Diisopropylethylamine → methyl 5-bromo-1-(2,6-dichlorophenyl)-2-oxo-1,4-dihydro-2H-3,1-benzoxazine-7-carboxylate

HRID 394215
ノート
印刷プレビュー

反応式

HRID 394215 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH:9]=[C:10](Br)[C:11]=1[CH2:12][O:13][C:14]([NH:16][C:17]1[C:22]([Cl:23])=[CH:21][CH:20]=[CH:19][C:18]=1[Cl:24])=[O:15])[C:5]([O:7][CH3:8])=[O:6].C(N(C(C)C)CC)(C)C>CN(C=O)C.[Cu]I>[Br:1][C:2]1[C:11]2[CH2:12][O:13][C:14](=[O:15])[N:16]([C:17]3[C:22]([Cl:23])=[CH:21][CH:20]=[CH:19][C:18]=3[Cl:24])[C:10]=2[CH:9]=[C:4]([C:5]([O:7][CH3:8])=[O:6])[CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 81531DiisopropylethylamineHCID 22648016Methyl 3,5-dibromo-4-[({[(2,6-dichlorophenyl)amino]carbonyl}oxy)methyl]benzoate

生成物 1

HCID 22647893methyl 5-bromo-1-(2,6-dichlorophenyl)-2-oxo-1,4-dihydro-2H-3,1-benzoxazine-7-carboxylate

試薬・触媒・溶媒 2

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)触媒HCID 6228
Dimethylformamide
溶媒

実験手順

To a solution of methyl 3,5-dibromo-4-[({[(2,6-dichlorophenyl)amino]carbonyl}oxy)methyl]benzoate (1 g, 1.96 mmol, 1 eq) in DMF (20 mL) was added CuI (411 mg, 2.16 mmol, 1.1 eq) and diisopropylethylamine (0.51 mL, 2.95 mmol, 1.5 eq). Degassed the reaction flask with argon and placed in a 140° C. oil bath. After 2.5 h the reaction was cooled. The mixture was filtered to remove inorganics. The solvent was removed under reduced pressure. The residue was dissolved in CH2Cl2, and washed with water. The aqueous layer was back-extracted 2× with CH2Cl2. The organic extracts were combined, dried over anhydrous Na2SO4, filtered and concentrated. The residue was triturated with Et2O leaving 283 mg of solid methyl 5-bromo-1-(2,6-dichlorophenyl)-2-oxo-1,4-dihydro-2H-3,1-benzoxazine-7-carboxylate. The supernatant was further purified by flash column chromatography on silica gel eluting with 2:1 CH2Cl2/hexanes giving an additional 309 mg of not quite pure product. Mass spectrum (ESI) 430.0 (M+1); 432.0 (M+3), 434.0 (M+5).

後処理

  1. customDegassed the reaction flask with argon
  2. customplaced in a 140° C.
  3. temperatureAfter 2.5 h the reaction was cooled
  4. filtrationThe mixture was filtered
  5. customto remove inorganics
  6. customThe solvent was removed under reduced pressure
  7. dissolutionThe residue was dissolved in CH2Cl2
  8. washwashed with water
  9. extractionThe aqueous layer was back-extracted 2× with CH2Cl2
  10. dry with materialdried over anhydrous Na2SO4
  11. filtrationfiltered
  12. concentrationconcentrated
  13. customThe residue was triturated with Et2O leaving 283 mg of solid methyl 5-bromo-1-(2,6-dichlorophenyl)-2-oxo-1,4-dihydro-2H-3,1-benzoxazine-7-carboxylate
  14. customThe supernatant was further purified by flash column chromatography on silica gel eluting with 2:1 CH2Cl2/hexanes giving an additional 309 mg of not quite pure product

出典と根拠

ORDレコード
ord-3c8d4c0eb2fd4acdac5cebd586795e82
出典データセット
uspto-grants-2004_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06809199B2

反応ノート

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