Benzyl Bromide → HCID 178459028、化合物

HRID 2255150ノート

反応式

HRID 2255150 の反応式
C(O[C:5]1[NH:10][C:9](=[O:11])[C:8]([CH2:12][CH:13]([CH3:15])[CH3:14])=[N+:7]([O-:16])[C:6]=1[NH2:17])C=C.[C:18](=O)([O-])[O-].[K+].[K+].[CH2:24](Br)[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1.[C:32]([O:35][CH2:36][CH3:37])(=O)C>CN(C)C=O>[CH2:36]([O:35][CH2:32][C:5]1[C:6]([NH2:17])=[N+:7]([O-:16])[C:8]([CH2:12][CH:13]([CH3:14])[CH3:15])=[C:9]([O:11][CH2:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[N:10]=1)[CH:37]=[CH2:18]

参加物

6

反応物 4

HCID 7498Benzyl BromideHCID 8857Ethyl AcetateHCID 11430Potassium CarbonateHCID 178458957HCID 178458957、化合物

生成物 1

HCID 178459028HCID 178459028、化合物

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

In 25 ml of dimethylformamide were dissolved 2.00 g of 6-allyloxy-5-amino-3-isobutyl-1,2-dihydropyrazin-2-one 4-oxide and 570 mg of potassium carbonate. Thereto was added 1.05 ml of benzyl bromide. The mixture was stirred for 1.5 hours at room temperature. After completion of the reaction, 200 ml of ethyl acetate was added to the reaction mixture. The resulting mixture was washed with water. The aqueous layer was extracted with 50 ml of ethyl acetate twice. The extract was combined with the above ethyl acetate layer. The combined mixture was washed with an aqueous solution saturated with NaCl, and dried with magnesium sulfate, then the solvent was removed by evaporation. The residue was purified by a silica gel column chromatography (eluting solvent: 40% by volume of ethyl acetate-n-hexane), followed by recrystallization from n-hexane to obtain 1.57 g of 3-allyloxymethyl-2-amino-5-benzyloxy-6-isobutylpyrazine 1-oxide (Compound B-4) as white fine needle-like crystals having a melting point of 56.3°-57.2° C.

後処理

  1. additionwas added to the reaction mixture
  2. washThe resulting mixture was washed with water
  3. extractionThe aqueous layer was extracted with 50 ml of ethyl acetate twice
  4. washThe combined mixture was washed with an aqueous solution saturated with NaCl
  5. dry with materialdried with magnesium sulfate
  6. customthe solvent was removed by evaporation
  7. customThe residue was purified by a silica gel column chromatography (eluting solvent: 40% by volume of ethyl acetate-n-hexane)
  8. customfollowed by recrystallization from n-hexane

出典と根拠

ORDレコード
ord-556bee671d7f494da990b150c997176f
出典データセット
uspto-grants-1993_08
特許番号
US05238938

反応ノート

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