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Sodium Sulfate → 6-[(4R)-4-{[3-(7-Methoxy-2-oxoquinoxalin-1(2H)-yl)propyl]amino}-2-oxopyrrolidin-1-yl]-2H-1,4-benzoxazin-3(4H)-one

HRID 1847030
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HRID 1847030 반응식
[NH2:1][C@H:2]1[CH2:6][N:5]([C:7]2[CH:8]=[CH:9][C:10]3[O:15][CH2:14][C:13](=[O:16])[NH:12][C:11]=3[CH:17]=2)[C:4](=[O:18])[CH2:3]1.[CH3:19][O:20][C:21]1[CH:30]=[C:29]2[C:24]([N:25]=[CH:26][C:27](=[O:35])[N:28]2[CH2:31][CH2:32][CH:33]=O)=[CH:23][CH:22]=1.S([O-])([O-])(=O)=O.[Na+].[Na+].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(=O)([O-])O.[Na+]>ClCCl>[CH3:19][O:20][C:21]1[CH:30]=[C:29]2[C:24]([N:25]=[CH:26][C:27](=[O:35])[N:28]2[CH2:31][CH2:32][CH2:33][NH:1][C@H:2]2[CH2:6][N:5]([C:7]3[CH:8]=[CH:9][C:10]4[O:15][CH2:14][C:13](=[O:16])[NH:12][C:11]=4[CH:17]=3)[C:4](=[O:18])[CH2:3]2)=[CH:23][CH:22]=1
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참가 물질

7

반응물 5

HCID 24436Sodium SulfateHCID 516892Sodium BicarbonateHCID 5049666Sodium triacetoxyborohydrideHCID 867249283-(7-Methoxy-2-oxoquinoxalin-1(2H)-yl)propanalHCID 867249576-[(4R)-4-Amino-2-oxopyrrolidin-1-yl]-2H-1,4-benzoxazin-3(4H)-one

생성물 1

HCID 60161776
6-[(4R)-4-{[3-(7-Methoxy-2-oxoquinoxalin-1(2H)-yl)propyl]amino}-2-oxopyrrolidin-1-yl]-2H-1,4-benzoxazin-3(4H)-one

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

6-[(4R)-4-Amino-2-oxopyrrolidin-1-yl]-2H-1,4-benzoxazin-3(4H)-one (23.9 mg, 0.0967 mmol) and 3-(7-methoxy-2-oxoquinoxalin-1(2H)-yl)propanal (Reference Example 8; 22.4 mg, 0.0967 mmol) were dissolved in N,N-dimethylfomamide (0.5 ml). Sodium sulfate (100 mg) was added to the obtained solution, and the mixture was then stirred at room temperature overnight. Thereafter, sodium triacetoxy borohydride (30.7 mg, 0.145 mmol) was added to the reaction solution, and the obtained mixture was then stirred at room temperature for 2 days. After completion of the reaction, dichloromethane and a saturated sodium hydrogen carbonate aqueous solution were added to the reaction solution, and the organic layer was separated. The organic layer was washed with water (4×) and saturated sodium chloride solution, and was then dried over anhydrous magnesium sulfate. Thereafter, the solvent was removed under reduced pressure. The obtained residue was purified by preparative thin layer chromatography (chloroform/methanol) to yield 18.4 mg (41%) of the above captioned compound in the form of a light brown solid.

후처리

  1. stirringthe obtained mixture was then stirred at room temperature for 2 days
  2. customthe organic layer was separated
  3. washThe organic layer was washed with water (4×) and saturated sodium chloride solution
  4. dry with materialwas then dried over anhydrous magnesium sulfate
  5. customThereafter, the solvent was removed under reduced pressure
  6. customThe obtained residue was purified by preparative thin layer chromatography (chloroform/methanol)
  7. customto yield 18.4 mg (41%) of the

출처 및 근거

ORD 기록
ord-d9677f2d28cc478ead824941648369ec
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08952010B2

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