Sodium hydride → Pyridin-3-yl-(pyridin-2-yloxy)-acetic acid ethyl ester

HRID 352226

反応式

HRID 352226 の反応式
[H-].[Na+].[OH:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][N:5]=1.[CH2:10]([O:12][C:13](=[O:22])[CH:14](Br)[C:15]1[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=1)[CH3:11]>CN(C=O)C>[CH2:10]([O:12][C:13](=[O:22])[CH:14]([C:15]1[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=1)[O:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][N:5]=1)[CH3:11]

参加物

5

実験手順

Sodium hydride (520 mg; 21.8 mmol; 1.4 equiv) was stirred with 2-hydroxypyridine (1.73 g; 18.2 mmol; 1.2 equiv) in DMF (30 mL) for 15 min. This solution was added to an aliquot of bromo-pyridin-3-yl-acetic acid ethyl ester (approx. 3.6 g; 15 mmol) in DMF (20 mL). After stirring overnight, at rt., the resulting opaque black solution was concentrated in vacuo, dissolved in 20% isopropyl alcohol/chloroform, washed 5 times with saturated NaHCO3(aq), washed twice with saturated NaCl(aq), and dried over Na2SO4(s). After filtration, the solution was concentrated in vacuo and purified by SiO2 column chromatography on two consecutive columns with a 1% methanol/chloroform mobile phase and then an ethyl acetate/hexanes mobile phase (30%, 40%, 50% step gradient). A light yellow oil (134 mg; approx. 3% yield) was isolated. MS(ES) calc'd: [M+H]+=259.2 m/z. Found: 259.1 m/z.

後処理

  1. concentration, the resulting opaque black solution was concentrated in vacuo
  2. dissolutiondissolved in 20% isopropyl alcohol/chloroform
  3. washwashed 5 times with saturated NaHCO3(aq)
  4. washwashed twice with saturated NaCl(aq)
  5. dry with materialdried over Na2SO4(s)
  6. filtrationAfter filtration
  7. concentrationthe solution was concentrated in vacuo
  8. custompurified by SiO2 column chromatography on two consecutive columns with a 1% methanol/chloroform mobile phase
  9. customA light yellow oil (134 mg; approx. 3% yield) was isolated

出典と根拠

ORDレコード
ord-d94fa65d735a4eb0a54115991fc4408a
出典データセット
uspto-grants-2004_06
特許番号
US06743794B2

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