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Methanol → HCID 178499647、化合物

HRID 1952355
ノート
印刷プレビュー

反応式

HRID 1952355 の反応式
[NH:1]1[C:5]2=[N:6][CH:7]=[CH:8][CH:9]=[C:4]2[C:3]([CH2:10][C:11]([OH:13])=[O:12])=[N:2]1.[CH3:14]O>Cl>[NH:1]1[C:5]2=[N:6][CH:7]=[CH:8][CH:9]=[C:4]2[C:3]([CH2:10][C:11]([O:13][CH3:14])=[O:12])=[N:2]1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 887MethanolHCID 178525255HCID 178525255、化合物

生成物 1

HCID 178499647HCID 178499647、化合物

試薬・触媒・溶媒 1

HCID 313Hydrochloric Acid溶媒

実験手順

To a solution of 1H-pyrazolo[3,4-b]pyridin-3-ylacetic acid (92 mg, 0.520 mmol) in methanol (4 mL) was bubbled in HCl gas for 2 minutes and the resulting solution was allowed to stand for a further 10 minutes. After this time, the solution was concentrated in vacuo and the resulting residue was partitioned between aqueous NaHCO3 (10 mL) and ethyl acetate (2×10 mL). The combined organic extracts were washed with brine, dried over MgSO4, filtered and the solvent evaporated in vacuo to provide the title compound. LRMS (M+1): 192.0.

後処理

  1. concentrationAfter this time, the solution was concentrated in vacuo
  2. customthe resulting residue was partitioned between aqueous NaHCO3 (10 mL) and ethyl acetate (2×10 mL)
  3. washThe combined organic extracts were washed with brine
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. customthe solvent evaporated in vacuo

出典と根拠

ORDレコード
ord-77d3ff586e91461981571b5880fd712e
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08404856B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート