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N-Iodosuccinimide → 3-iodo-2-methyl-1H-pyrrolo[2,3-c]pyridine

HRID 588412
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 588412
[CH3:1][C:2]1[NH:10][C:5]2=[CH:6][N:7]=[CH:8][CH:9]=[C:4]2[CH:3]=1.[I:11]N1C(=O)CCC1=O>C(Cl)(Cl)Cl>[I:11][C:3]1[C:4]2[C:5](=[CH:6][N:7]=[CH:8][CH:9]=2)[NH:10][C:2]=1[CH3:1]
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Komponenten

4

Edukt 2

HCID 120273N-IodosuccinimideHCID 124075052-Methyl-1H-pyrrolo(2,3-c)pyridine

Produkt 1

HCID 674185123-iodo-2-methyl-1H-pyrrolo[2,3-c]pyridineAusbeute 92 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6212ChloroformLösungsmittel

Versuchsvorschrift

2-Methyl-1H-pyrrolo[2,3-c]pyridine (100 mg, 0.76 mmol) was dissolved in CHCl3 (5 mL), N-iodosuccinimide (179 mg, 0.79 mmol) was added and the reaction mixture was stirred for 2 h. The reaction mixture was quenched with 1 M aq sodium thiosulphate (5 mL) and the CHCl3 was removed in vacuo. The reaction mixture was partitioned between sat aq NaHCO3 (40 mL) and EtOAc (40 mL). The aqueous layer was extracted with EtOAc (40 mL) and the combined organic fractions were washed with sat aq NaHCO3 (50 mL) and brine (50 mL), dried (MgSO4) and concentrated in vacuo to give the title compound as a cream solid (179 mg, 92%). LCMS (ES+): 258.9 (M+H)+.

Aufarbeitung

  1. customThe reaction mixture was quenched with 1 M aq sodium thiosulphate (5 mL)
  2. customthe CHCl3 was removed in vacuo
  3. customThe reaction mixture was partitioned
  4. extractionThe aqueous layer was extracted with EtOAc (40 mL)
  5. washthe combined organic fractions were washed with sat aq NaHCO3 (50 mL) and brine (50 mL)
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-0bc03b6cdbca44099e42bb0342e9bb07
Quelldatensatz
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09227967B2

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