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Potassium Carbonate → 6-(Methyloxy)-4-{2-[(2S)-2-oxiranyl]ethyl}pyrido[2,3-b]pyrazin-3(4H)-one

HRID 1847065
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HRID 1847065 반응식
CC1C=CC(S(O[CH2:12][C@@H:13]([OH:29])[CH2:14][CH2:15][N:16]2[C:21](=[O:22])[CH:20]=[N:19][C:18]3[CH:23]=[CH:24][C:25]([O:27][CH3:28])=[N:26][C:17]2=3)(=O)=O)=CC=1.C(=O)([O-])[O-].[K+].[K+]>CO>[CH3:28][O:27][C:25]1[CH:24]=[CH:23][C:18]2[N:19]=[CH:20][C:21](=[O:22])[N:16]([CH2:15][CH2:14][C@H:13]3[CH2:12][O:29]3)[C:17]=2[N:26]=1
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참가 물질

4

반응물 2

HCID 11430Potassium CarbonateHCID 86724989(2S)-2-hydroxy-4-(6-methoxy-3-oxopyrido[2,3-b]pyrazin-4(3H)-yl)butyl 4-methylbenzenesulfonate

생성물 1

HCID 866497106-(Methyloxy)-4-{2-[(2S)-2-oxiranyl]ethyl}pyrido[2,3-b]pyrazin-3(4H)-one수율 62.2%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

In methanol (15 ml) was dissolved (2S)-2-hydroxy-4-(6-methoxy-3-oxopyrido[2,3-b]pyrazin-4(3H)-yl)butyl 4-methylbenzenesulfonate (227 mg, 0.540 mmol), and potassium carbonate (90 mg, 0.648 mmol) was then added to the solution at room temperature. The obtained mixture was stirred for 17 hours. Thereafter, the solvent was removed from the reaction solution under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform/methanol) to yield 83 mg (62%) of the above-captioned compound in the form of a yellow solid.

후처리

  1. additionwas then added to the solution at room temperature
  2. customThereafter, the solvent was removed from the reaction solution under reduced pressure
  3. customThe obtained residue was purified by silica gel column chromatography (chloroform/methanol)

출처 및 근거

ORD 기록
ord-8206dbe5f6d349a6af6c6752a8445cdc
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08952010B2

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