ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Hydrochloric Acid → (1-Methyl-6-oxo-1,6-dihydropyridin-3-yl)boronic acid

HRID 385930
ノート
印刷プレビュー

反応式

HRID 385930 の反応式
Br[C:2]1[CH:3]=[CH:4][C:5](=[O:9])[N:6]([CH3:8])[CH:7]=1.C1(P(C2CCCCC2)C2CCCCC2)CCCCC1.CC1(C)C(C)(C)[O:33][B:32](B2OC(C)(C)C(C)(C)O2)[O:31]1.C([O-])(=O)C.[K+].Cl>C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[CH3:8][N:6]1[C:5](=[O:9])[CH:4]=[CH:3][C:2]([B:32]([OH:33])[OH:31])=[CH:7]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 313Hydrochloric AcidHCID 75806TricyclohexylphosphineHCID 517044Potassium AcetateHCID 2733548Bis(pinacolato)diboraneHCID 130240275-Bromo-1-methylpyridin-2(1H)-one

生成物 1

HCID 59526383(1-Methyl-6-oxo-1,6-dihydropyridin-3-yl)boronic acid

試薬・触媒・溶媒 1

HCID 9811564Bis(dibenzylideneacetone)palladium触媒

反応条件

温度
90 °C

実験手順

5-Bromo-1-methylpyridin-2(1H)-one (400 mg, 2.17 mmol), tricyclohexylphosphine (72 mg, 0.26 mmol), 4,4,4′,4′,5,5,5′,5′-octamethyl-2,2′-bi-1,3,2-dioxaborolane (540 mg, 2.17 mmol), potassium acetate (522 mg, 5.32 mmol) and Pd2(dba)3 (97 mg, 0.11 mmol) were added to a flask. The flask was evacuated and purged with argon three times. Fully degassed dioxane (9.5 mL) was added and the reaction was sealed and heated at 90° C. overnight. The mixture was then cooled to room temperature, filtered over a thin layer of celite, eluting with dichloromethane. The majority of the dichloromethane was evaporated under reduced pressure and hexane was added until a precipitate formed. The slurry was filtered and the filtrate was concentrated. The resulting residue was dissolved in dioxane, 10 equivalents of 1 N hydrochloric acid were added, and the mixture was stirred overnight. Removal of the solvent under reduced pressure and purification of the resulting residue via reverse phase HPLC (10-100% acetonitrile/water+0.05% TFA modifier) afforded the title compound.

後処理

  1. customThe flask was evacuated
  2. custompurged with argon three times
  3. additionFully degassed dioxane (9.5 mL) was added
  4. customthe reaction was sealed
  5. temperatureThe mixture was then cooled to room temperature
  6. filtrationfiltered over a thin layer of celite,
  7. washeluting with dichloromethane
  8. customThe majority of the dichloromethane was evaporated under reduced pressure and hexane
  9. additionwas added until a precipitate
  10. customformed
  11. filtrationThe slurry was filtered
  12. concentrationthe filtrate was concentrated
  13. dissolutionThe resulting residue was dissolved in dioxane
  14. customRemoval of the solvent
  15. customunder reduced pressure and purification of the resulting residue via reverse phase HPLC (10-100% acetonitrile/water+0.05% TFA modifier)

出典と根拠

ORDレコード
ord-2d6f90f1d77d484cbd87362308b2ec98
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08367706B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート