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O-Methylhydroxylamine → furo[2,3-c]pyridazin-5(6H)-one O-methyl oxime

HRID 1508194
ノート
印刷プレビュー

反応式

HRID 1508194 の反応式
[N:1]1[C:6]2[O:7][CH2:8][C:9](=O)[C:5]=2[CH:4]=[CH:3][N:2]=1.[CH3:11][O:12][NH2:13].CC([O-])=O.[Na+]>CCO>[CH3:11][O:12][N:13]=[C:9]1[C:5]2[CH:4]=[CH:3][N:2]=[N:1][C:6]=2[O:7][CH2:8]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

5

反応物 3

HCID 4113O-MethylhydroxylamineHCID 517045Sodium AcetateHCID 86721900furo[2,3-c]pyridazin-5(6H)-one

生成物 1

HCID 86721901furo[2,3-c]pyridazin-5(6H)-one O-methyl oxime

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
30 °C

実験手順

To a solution of furo[2,3-c]pyridazin-5(6H)-one (4.81 mmol) in 30 mL EtOH were added O-methyl-hydroxylamine (9.62 mmol) and NaOAc (9.62 mmol). After heating to 30° C. for 4.5 h the reaction mixture was concentrated in vacuo to half of its volume. Water and DCM were added and the aqueous phase was extracted with DCM (3×). The combined organic layers were dried over MgSO4 and concentrated in vacuo. Purification by CC (KP-SIL™ from Biotage) using Hept/EtOAc (1/1) gives the desired product as beige solid;

後処理

  1. concentrationwas concentrated in vacuo to half of its volume
  2. additionWater and DCM were added
  3. extractionthe aqueous phase was extracted with DCM (3×)
  4. dry with materialThe combined organic layers were dried over MgSO4
  5. concentrationconcentrated in vacuo
  6. customPurification by CC (KP-SIL™ from Biotage)

出典と根拠

ORDレコード
ord-851114f8ad8b4b6d851cb0ff957e60ef
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09221832B2

反応ノート

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