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Methanol → (((4-Ethyl-2,3-dioxopiperazin-1-yl)carbonyl)amino)(4-hydroxyphenyl)acetic acid

HRID 67699
ノート
印刷プレビュー

反応式

HRID 67699 の反応式
OC1C=CC([NH:8][CH2:9][C:10]([OH:12])=[O:11])=CC=1.C[Si]([CH:17]([Si](C)(C)C)[C:18](N)=O)(C)C.[CH2:25]1[O:28][CH:26]1[CH3:27].[CH2:29]([N:31]1[CH2:36][CH2:35][N:34]([C:37](Cl)=[O:38])[C:33](=[O:40])[C:32]1=[O:41])[CH3:30].[CH3:42]O>C1COCC1>[CH2:29]([N:31]1[CH2:36][CH2:35][N:34]([C:37]([NH:8][CH:9]([C:18]2[CH:17]=[CH:27][C:26]([OH:28])=[CH:25][CH:42]=2)[C:10]([OH:12])=[O:11])=[O:38])[C:33](=[O:40])[C:32]1=[O:41])[CH3:30]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 887MethanolHCID 6378Propylene OxideHCID 67149N-(4-Hydroxyphenyl)glycineHCID 1088134-Ethyl-2,3-dioxopiperazinecarbonyl chlorideHCID 11708267Bistrimethylsilylacetamid

生成物 1

HCID 3018895(((4-Ethyl-2,3-dioxopiperazin-1-yl)carbonyl)amino)(4-hydroxyphenyl)acetic acid収率 40%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
0 °C

実験手順

To a suspension of 8.3 g. (50 mmole) of 4-hydroxyphenylglycine in 75 ml. of tetrahydrofuran were added 25 ml. of bis-trimethylsilylacetamide and the suspension was stirred at room temperature for 15 minutes and then at 75° C. for 2.5 hours to form a solution. The solution was cooled to 0° C. and 25 ml. of propylene oxide were added. Next a solution of 11 g. of 4-ethylpiperazin-2,3-dione-1-ylcarbonyl chloride in 100 ml. of THF was added and the reaction mixture was stirred for 1 hour at 0° C. and at room temperature for 4 hours. Methyl alcohol, 40 ml., were added to the reaction mixture and after stirring for 15 minutes the mixture was evaporated to dryness. The gummy residue was dissolved in a mixture of ethyl acetate-aqueous sodium bicarbonate and the aqueous layer was separated, washed with ethyl acetate, filtered, and cooled to 0° C. The cold solution was layered with 200 ml. of fresh ethyl acetate and the pH adjusted to pH 1.9 with concentrated hydrochloric acid. The organic phase was separated, combined with an ethyl acetate wash of the acidified aqueous phase and dried over sodium sulfate. Evaporation of the dried organic phase gave 6.7 g. (40% yield) of α-(4-ethylpiperazin-2,3-dione-1-ylcarbonylamino)-4-hydroxyphenylacetic acid.

後処理

  1. additionTo a suspension of 8.3 g
  2. customat 75° C. for 2.5 hours to form a solution
  3. addition, were added to the reaction mixture
  4. stirringafter stirring for 15 minutes the mixture
  5. customwas evaporated to dryness
  6. dissolutionThe gummy residue was dissolved in a mixture of ethyl acetate-aqueous sodium bicarbonate
  7. customthe aqueous layer was separated
  8. washwashed with ethyl acetate
  9. filtrationfiltered
  10. temperaturecooled to 0° C
  11. customThe organic phase was separated
  12. washwash of the acidified aqueous phase
  13. dry with materialdried over sodium sulfate
  14. customEvaporation of the dried organic phase
  15. customgave 6.7 g

出典と根拠

ORDレコード
ord-742c8fd720994516bfdd1a5645a8e425
出典データセット
uspto-grants-1982_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04346076

反応ノート

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