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Isopropanol → 5-(Propan-2-yloxy)pyrazine-2-carboxylic acid

HRID 1526599
ノート
印刷プレビュー

反応式

HRID 1526599 の反応式
[CH3:1][C:2](C)([O-:4])[CH3:3].[Na+].CC(O)C.Cl[C:12]1[N:13]=[CH:14][C:15]([C:18]([O:20]C)=[O:19])=[N:16][CH:17]=1>C1COCC1>[CH:2]([O:4][C:12]1[N:13]=[CH:14][C:15]([C:18]([OH:20])=[O:19])=[N:16][CH:17]=1)([CH3:3])[CH3:1]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 3776IsopropanolHCID 406081Methyl 5-chloropyrazine-2-carboxylateHCID 23676156Sodium t-butoxide

生成物 1

HCID 642663795-(Propan-2-yloxy)pyrazine-2-carboxylic acid

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a rt solution of sodium t-butoxide (1.41 g, 14.67 mmol) in THF (20 mL) was added 2-propanol (1.250 mL, 16.33 mmol) dropwise. After 10 min a solution of methyl 5-chloro-2-pyrazinecarboxylate (1.70 g, 9.85 mmol, Ark Pharm) in THF (10 mL) was added dropwise. After 1.5 h, the reaction was quenched with saturated aq NH4Cl and extracted with EtOAc (3×). The aqueous layer was concentrated under reduced pressure and the resulting solid was treated with aqueous HCl. The solution was extracted with DCM (3×) and the combined organic layers were purified by flash chromatography, eluting with 0.5% TFA in iPrOH:CH2Cl2 (0:1→1:9) to give a white crystalline solid. (497 mg, 2.7 mmol, 28%). MS m/z=183 [M+H]+. Calculated for C8H10N2O3: 182.

後処理

  1. customthe reaction was quenched with saturated aq NH4Cl
  2. extractionextracted with EtOAc (3×)
  3. concentrationThe aqueous layer was concentrated under reduced pressure
  4. additionthe resulting solid was treated with aqueous HCl
  5. extractionThe solution was extracted with DCM (3×)
  6. customthe combined organic layers were purified by flash chromatography
  7. washeluting with 0.5% TFA in iPrOH:CH2Cl2 (0:1→1:9)
  8. customto give a white crystalline solid

出典と根拠

ORDレコード
ord-f023f1e1f64140c9932d6d2f59958a10
出典データセット
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09085576B2

反応ノート

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