Benzyl Bromide → HCID 178459028, 화합물

HRID 2255150노트

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HRID 2255150 반응식
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]

참가 물질

6

반응물 4

HCID 7498Benzyl BromideHCID 8857Ethyl AcetateHCID 11430Potassium CarbonateHCID 178458957HCID 178458957, 화합물

생성물 1

HCID 178459028HCID 178459028, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-556bee671d7f494da990b150c997176f
출처 데이터셋
uspto-grants-1993_08
특허 번호
US05238938

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