Hydrochloric Acid → 4-Thiazolecarboxylic acid, 2-propyl-, ethyl ester

HRID 471111ノート

反応式

HRID 471111 の反応式
Cl.[C:2]([NH:7][CH:8]([CH2:14][SH:15])[C:9]([O:11][CH2:12][CH3:13])=[O:10])(=O)[CH2:3][CH2:4][CH3:5]>C(O)C>[CH2:3]([C:2]1[S:15][CH:14]=[C:8]([C:9]([O:11][CH2:12][CH3:13])=[O:10])[N:7]=1)[CH2:4][CH3:5]

参加物

4

反応物 2

HCID 313Hydrochloric AcidHCID 57989348Ethyl 2-butyramido-3-mercaptopropanoate

生成物 1

HCID 2036314-Thiazolecarboxylic acid, 2-propyl-, ethyl ester

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A solution of HCl (4M in 1,4-dioxane, 20 mL) was added to a solution of ethyl 2-butyramido-3-mercaptopropanoate (example 56, step a) (3 g) in ethanol (20 mL) and the resulting mixture stirred overnight. The solvent was evaporated and the residue azeotroped twice with toluene. The residue was redissolved in acetonitrile (50 mL), manganese dioxide (11.9 g) was added and the mixture heated at reflux overnight. The reaction was filtered through a pad of Celite. The filter pad was washed with MeCN (3×100 mL). The combined filtrate and washings were evaporated and the residue was purified by silica gel chromatography eluting with 9:1 isohexane:ethyl acetate. The product containing fractions were combined and evaporated to give the subtitled compound as a clear oil. Yield 0.24 g.

後処理

  1. customThe solvent was evaporated
  2. customthe residue azeotroped twice with toluene
  3. dissolutionThe residue was redissolved in acetonitrile (50 mL)
  4. additionmanganese dioxide (11.9 g) was added
  5. temperaturethe mixture heated
  6. temperatureat reflux overnight
  7. filtrationThe reaction was filtered through a pad of Celite
  8. washThe filter pad was washed with MeCN (3×100 mL)
  9. customThe combined filtrate and washings were evaporated
  10. customthe residue was purified by silica gel chromatography
  11. washeluting with 9:1 isohexane
  12. additionThe product containing fractions
  13. customevaporated

出典と根拠

ORDレコード
ord-86747565f67d4e899d44e38c80d5e855
出典データセット
uspto-grants-2014_01
特許番号
US08629271B2

反応ノート

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