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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
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1,4-Dioxane--water (1/1) → HCID 178519752、化合物

HRID 2374161
ノート
印刷プレビュー

反応式

HRID 2374161 の反応式
[CH:1]1([C:4]2[NH:13][C:7]3=[N:8][CH:9]=[CH:10][C:11]([CH3:12])=[C:6]3[N:5]=2)[CH2:3][CH2:2]1.[O:14]1CCOCC1.O>>[CH:1]1([C:4]2[NH:13][C:7]3=[N:8][CH:9]=[CH:10][C:11]([CH:12]=[O:14])=[C:6]3[N:5]=2)[CH2:3][CH2:2]1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 218864351,4-Dioxane--water (1/1)HCID 178428356HCID 178428356、化合物

生成物 1

HCID 178519752HCID 178519752、化合物

実験手順

2-Cyclopropyl-7-methyl-3H-imidazo[4,5-b]pyridine (100 mg, 0.58 mmol; from EP0420237 A1) was treated with SeO2 (160 mg, 1.44 mmol) in 6 ml of dioxane:water (4:1) and subjected to microwave irradiation (300 W, normal absorbance) at 180° C. for three 20 min interyals. The mixture was subsequently treated with satd. aq. NaHCO3 (25 ml) and water (25 ml) and the solids were removed by filtration through Celite, rinsing with DCM. The filtrate was extracted with DCM (4×50 mL) and the combined organic extracts were dried (Na2SO4), filtered, and concentrated to dryness to yield the crude title compound. MS (ESI+) for m/z 188 (M+H)+.

後処理

  1. customsubjected to microwave irradiation (300 W, normal absorbance) at 180° C. for three 20 min interyals
  2. additionThe mixture was subsequently treated with satd
  3. customaq. NaHCO3 (25 ml) and water (25 ml) and the solids were removed by filtration through Celite
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
  • washrinsing with DCM
  • extractionThe filtrate was extracted with DCM (4×50 mL)
  • dry with materialthe combined organic extracts were dried (Na2SO4)
  • filtrationfiltered
  • concentrationconcentrated to dryness
  • 出典と根拠

    ORDレコード
    ord-c7164df1ca0d4e3cb01416dbd3f1de79
    出典データセット
    uspto-grants-2008_12
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US07462600B2

    反応ノート

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