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ethyl 1H-pyrrolo[2,3-c]pyridine-2-carboxylate → HCID 20158234、化合物

HRID 2080540
ノート
印刷プレビュー

反応式

HRID 2080540 の反応式
[NH:1]1[C:5]2=[CH:6][N:7]=[CH:8][CH:9]=[C:4]2[CH:3]=[C:2]1[C:10]([O:12][CH2:13][CH3:14])=[O:11]>C(O)(=O)C.[Rh]>[NH:1]1[C:5]2[CH2:6][NH:7][CH2:8][CH2:9][C:4]=2[CH:3]=[C:2]1[C:10]([O:12][CH2:13][CH3:14])=[O:11]
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 1

HCID 21819001ethyl 1H-pyrrolo[2,3-c]pyridine-2-carboxylate

生成物 1

HCID 20158234HCID 20158234、化合物収率 97%

試薬・触媒・溶媒 2

HCID 23948Rhodium触媒HCID 176Acetic Acid溶媒

実験手順

Ethyl 1H-pyrrolo[2,3-c]pyridine-2-carboxylate (4.225 g, 22.21 mmol) was dissolved in acetic acid (150 mL) and 5% Rh/Al2O3 (9.144 g, 0.2 eq.) was added. The suspension was hydrogenated (45 Bars) at rt for 4 days then at 50° C. for 7 days. The catalyst was removed by filtration through a Celite pad, was washed with acetic acid and the filtrate was evaporated. The residue was dissolved in DCM, washed with saturated aqueous solution of NaHCO3 and aqueous phases were extracted with DCM. The combined organic layers were washed with brine, dried over Na2SO4 and concentrated to give the title compound (4.183 g, 97%). HPLC purity: 92%. M+(LC-MS (ESI)): 195, M−(LC-MS (ESI)): 193

後処理

  1. customat rt
  2. customfor 4 days
  3. customThe catalyst was removed by filtration through a Celite pad
  4. washwas washed with acetic acid
  5. customthe filtrate was evaporated
  6. dissolutionThe residue was dissolved in DCM
  7. washwashed with saturated aqueous solution of NaHCO3 and aqueous phases
  8. extractionwere extracted with DCM
  9. washThe combined organic layers were washed with brine
  10. dry with materialdried over Na2SO4
  11. concentrationconcentrated

出典と根拠

ORDレコード
ord-7feeb1bbe6c143e4b92c42dadc3764a6
出典データセット
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07932389B2

反応ノート

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