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Water → 5-Ethynyl-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acid (1-(S)-dimethylcarbamoyl-2-phenyl ethyl)amide

HRID 751708
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 751708
Cl.[NH2:2][C@@H:3]([CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[C:4]([N:6]([CH3:8])[CH3:7])=[O:5].CC[N:18]([CH:22]([CH3:24])[CH3:23])[CH:19]([CH3:21])[CH3:20].C1C=[CH:27][C:28]2N(O)N=[N:31][C:29]=2[CH:30]=1.[OH2:35].CCN=C=NCCCN(C)C>CN(C=O)C>[CH3:7][N:6]([CH3:8])[C:4]([C@@H:3]([NH:2][C:21]([C:19]1[NH:18][C:22]2=[CH:23][N:31]=[C:29]([C:28]#[CH:27])[CH:30]=[C:24]2[CH:20]=1)=[O:35])[CH2:9][C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1)=[O:5]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 5

HCID 962WaterHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 12653778(2S)-2-Amino-N,N-dimethyl-3-phenylpropanamide hydrochloride

Produkt 1

HCID 59753683
5-Ethynyl-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acid (1-(S)-dimethylcarbamoyl-2-phenyl ethyl)amide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

To a solution of 2-(S)-amino-N,N-dimethyl-3-phenylpropionamide hydrochloride (Preparation 8, 0.0135 g, 0.059 mmol) in DMF (anhydrous, 3 mL) was added DIPEA (0.031 mL, 0.177 mmol) then carboxylic acid (Preparation 60, 0.010 g, 0.054 mmol). To the stirred solution was added HOBt.H2O (0.008 g, 0.059 mmol) then, after 10 min, EDCI (0.012 g, 0.065 mmol). The reaction mixture was stirred for 18 h then all volatiles were removed in vacuo. The residue was partitioned between ethyl acetate (30 mL) and water (20 mL). The layers were separated and the aqueous layer extracted with ethyl acetate (3×20 mL). The combined organics were washed with brine (30 mL), dried (MgSO4), filtered and concentrated in vacuo. The residue was dissolved in methanol then adsorbed onto silica gel. Purification via flash column chromatography (SiO2, CH2Cl2:MeOH, 19:1, v/v) gave the title compound as an off-white solid. δH (CD3OD): 2.88 (3H, s), 2.89 (3H, s), 3.00–3.23 (2H, m), 3.50 (1H, s), 5.27 (1H, t), 7.10–7.37 (6H, m), 7.86 (1H, s), 8.70 (1H, s). m/z (ES+)=361 [M+H]+; RT=2.65 min.

Aufarbeitung

  1. customall volatiles were removed in vacuo
  2. customThe residue was partitioned between ethyl acetate (30 mL) and water (20 mL)
  3. customThe layers were separated
  4. extractionthe aqueous layer extracted with ethyl acetate (3×20 mL)
  5. washThe combined organics were washed with brine (30 mL)
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. dissolutionThe residue was dissolved in methanol
  10. customPurification via flash column chromatography (SiO2, CH2Cl2

Quellen und Nachweise

ORD-Eintrag
ord-cb13b6af6b7547fe9437a6afc2ada4d5
Quelldatensatz
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07405210B2

Notizen zur Reaktion

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