Acetic Acid → HCID 178486771、化合物

HRID 1791542ノート

反応式

HRID 1791542 の反応式
Cl.[NH2:2][C:3]1[CH:11]=[C:10]([O:12][CH2:13][CH2:14][CH2:15][N:16]2[CH2:20][CH2:19][CH2:18][CH2:17]2)[C:9]([O:21][CH3:22])=[CH:8][C:4]=1[C:5]([NH2:7])=[O:6].[CH3:23]N(C=NC=[N+](C)C)C.[Cl-].C(O)(=O)C.C([O-])(=O)C.[Na+]>O1CCOCC1>[OH:6][C:5]1[C:4]2[C:3](=[CH:11][C:10]([O:12][CH2:13][CH2:14][CH2:15][N:16]3[CH2:20][CH2:19][CH2:18][CH2:17]3)=[C:9]([O:21][CH3:22])[CH:8]=2)[N:2]=[CH:23][N:7]=1

参加物

6

実験手順

A mixture of 2-amino-5-methoxy-4-(3-(pyrrolidin-1-yl)propoxy)benzamide hydrochloride (5.92 g, 16.2 mmol) and Gold's reagent (3.5 g, 21.4 mmol) in dioxane (50 ml) was heated at reflux for 5 hours. Acetic acid (0.7 ml) and sodium acetate (1.33 g) were added to the reaction mixture which was heated at reflux for a further 5 hours. The mixture was allowed to cool and the volatiles were removed by evaporation. The residue was dissolved in water, adjusted to pH8 with 2M aqueous sodium hydroxide solution and purified on a Diaion (trademark of Mitsubishi) HP20SS resin column eluting with methanol (gradient 0–50%) in water. The fractions containing product were concentrated by evaporation and then freeze dried to give 4-hydroxy-6-methoxy-7-(3-(pyrrolidin-1-yl)propoxy)quinazoline (4.55 g, 83%).

後処理

  1. temperaturewas heated
  2. temperatureat reflux for 5 hours
  3. temperaturewas heated
  4. temperatureat reflux for a further 5 hours
  5. temperatureto cool
  6. customthe volatiles were removed by evaporation
  7. dissolutionThe residue was dissolved in water
  8. custompurified on a Diaion (trademark of Mitsubishi) HP20SS resin column
  9. washeluting with methanol (gradient 0–50%) in water
  10. additionThe fractions containing product
  11. concentrationwere concentrated by evaporation
  12. customfreeze dried

出典と根拠

ORDレコード
ord-e8213d2577f9480c993b2fc592165aac
出典データセット
uspto-grants-2006_07
特許番号
US07074800B1

反応ノート

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