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Benzyl Bromide → Quinoline-6-carboxylic acid (2-benzyl-2H-tetrazol-5-ylmethyl)-amide

HRID 2080243
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2080243
[N-]=[N+]=[N-].[Na+].[Cl-].[NH4+].C(CNC(C1C=C2C(=CC=1)N=CC=C2)=O)#N.[CH2:23](Br)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.C(=O)([O-])[O-].[K+].[K+].[N:37]1[NH:38][N:39]=[N:40][C:41]=1[CH2:42][NH:43][C:44]([C:46]1[CH:47]=[C:48]2[C:53](=[CH:54][CH:55]=1)[N:52]=[CH:51][CH:50]=[CH:49]2)=[O:45]>CN(C)C=O.C(OCC)(=O)C.O>[CH2:23]([N:38]1[N:39]=[N:40][C:41]([CH2:42][NH:43][C:44]([C:46]2[CH:47]=[C:48]3[C:53](=[CH:54][CH:55]=2)[N:52]=[CH:51][CH:50]=[CH:49]3)=[O:45])=[N:37]1)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

10

Edukt 6

HCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 25517Ammonium ChlorideHCID 33557Sodium AzideHCID 55126745quinoline-6-carboxylic acid (2H-tetrazol-5-ylmethyl)amideHCID 58388078Quinoline-6-carboxylic acid cyanomethyl-amide

Produkt 1

HCID 58875321
Quinoline-6-carboxylic acid (2-benzyl-2H-tetrazol-5-ylmethyl)-amide

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 962WaterLösungsmittelHCID 6228DimethylformamideLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

Sodium azide (260 mg, 4.0 mmol) and ammonium chloride (210 mg, 4.0 mmol) were suspended in a solution of quinoline-6-carboxylic acid cyanomethyl-amide described in Preparation Example E-1 (420 mg, 2.0 mmol) in N,N-dimethylformamide (15 mL), and the solution was stirred at 100° C. for 12 hours. Benzyl bromide (0.12 mL, 1.0 mmol) and potassium carbonate (400 mg, 3.0 mmol) were added to a solution having half the amount of the solution containing quinoline-6-carboxylic acid (2H-tetrazol-5-ylmethyl)amide obtained, which was then stirred for 20 minutes at 50° C. Water and ethyl acetate were added to the reaction solution, which was then partitioned, NH silica gel was added to the organic layer, and the solvent was evaporated in vacuo for adsorption, purification was carried out by NH silica gel column chromatography, and the title compound (20 mg, 0.058 mmol) was obtained as a white solid.

Aufarbeitung

  1. customobtained
  2. stirringwhich was then stirred for 20 minutes at 50° C
  3. customwas then partitioned
  4. additionNH silica gel was added to the organic layer
  5. customthe solvent was evaporated in vacuo for adsorption, purification

Quellen und Nachweise

ORD-Eintrag
ord-1408cdae9fdb44e2905ac3ed7aff3acb
Quelldatensatz
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07932272B2

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