Dicyclohexylcarbodiimide → Methyl 3-[(4-bromo-2-fluorophenyl)amino]-2-methoxy-3-oxopropanoate

HRID 487007ノート

反応式

HRID 487007 の反応式
[CH3:1][O:2][CH:3]([C:8]([O-:10])=O)[C:4]([O:6][CH3:7])=[O:5].[Br:11][C:12]1[CH:18]=[CH:17][C:15]([NH2:16])=[C:14]([F:19])[CH:13]=1.C1(N=C=NC2CCCCC2)CCCCC1>O1CCCC1>[Br:11][C:12]1[CH:18]=[CH:17][C:15]([NH:16][C:8](=[O:10])[CH:3]([O:2][CH3:1])[C:4]([O:6][CH3:7])=[O:5])=[C:14]([F:19])[CH:13]=1

参加物

5

反応物 3

HCID 10868DicyclohexylcarbodiimideHCID 1230504-Bromo-2-fluoroanilineHCID 229990802,3-Dimethoxy-3-oxopropanoate

生成物 1

HCID 19096850Methyl 3-[(4-bromo-2-fluorophenyl)amino]-2-methoxy-3-oxopropanoate

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a stirred mixture of 2.78 grams (0.02 mole) of monomethyl methoxymalonate prepared in Example LVI (Compound 214) and 3.56 grams (0.02 mole) of 4-bromo-2-fluoroaniline in approximately 100 milliliters of dry tetrahydrofuran was fed dropwise a solution of 3.87 grams (0.02 mole) of 1,3-dicyclohexylcarbodiimide in about 30 milliliters of dry tetrahydrofuran, while cooling the reaction mixture in an ice-water bath. The reaction mixture was allowed to warm slowly to room temperature and stirring continued for an approximate 65-hour period. The precipitated 1,3-dicyclohexylurea by-product (3.15 grams) was removed by filtration and the filtrate vacuum evaporated and the residue dissolved in methylene chloride. The latter solution was extracted with dilute HCl and then water, then dried (MgSO4) and solvent vacuum evaporated to give a colorless liquid. Flash column chromatography of the latter on silica, eluting with hexane-ethyl acetate (7:3) gave, after workup, a liquid which crystallized on standing. Recrystallization from hexane containing a small amount of ethyl acetate gave 2.3 grams (0.01 mole) of methyl 3-[(4-bromo-2-fluorophenyl)amino]-2-methoxy-3-oxopropanaote having a melting point of 51° C.-53° C. Elemental analysis of the product indicated the following:

後処理

  1. temperaturewhile cooling the reaction mixture in an ice-water bath
  2. waitcontinued for an approximate 65-hour period
  3. customThe precipitated 1,3-dicyclohexylurea by-product (3.15 grams) was removed by filtration
  4. customthe filtrate vacuum evaporated
  5. dissolutionthe residue dissolved in methylene chloride
  6. extractionThe latter solution was extracted with dilute HCl
  7. dry with materialwater, then dried (MgSO4) and solvent vacuum
  8. customevaporated
  9. customto give a colorless liquid
  10. washFlash column chromatography of the latter on silica, eluting with hexane-ethyl acetate (7:3)
  11. customgave
  12. customafter workup, a liquid which crystallized
  13. customRecrystallization from hexane containing a small amount of ethyl acetate
  14. customgave 2.3 grams (0.01 mole) of methyl 3-[(4-bromo-2-fluorophenyl)amino]-2-methoxy-3-oxopropanaote having a melting point of 51° C.-53° C

出典と根拠

ORDレコード
ord-e6bc91792a2f4e5c8d1d9d37684f955f
出典データセット
uspto-grants-1994_03
特許番号
US05292937

反応ノート

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