Ammonium Hydroxide → 1-propyl-5-(tetrahydro-2H-pyran-4-ylmethyl)-1H-pyrazole-3-carboxamide

HRID 549238Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 549238
Cl.C[N:3](C)CCCN=C=NCC.[CH2:13]([N:16]1[C:20]([CH2:21][CH:22]2[CH2:27][CH2:26][O:25][CH2:24][CH2:23]2)=[CH:19][C:18]([C:28]([OH:30])=O)=[N:17]1)[CH2:14][CH3:15].ON1C2C=CC=CC=2N=N1.[OH-].[NH4+]>CN(C)C=O.O>[CH2:13]([N:16]1[C:20]([CH2:21][CH:22]2[CH2:27][CH2:26][O:25][CH2:24][CH2:23]2)=[CH:19][C:18]([C:28]([NH2:3])=[O:30])=[N:17]1)[CH2:14][CH3:15]

Komponenten

7

Versuchsvorschrift

1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (4.06 g, 21.2 mmol) was added to a solution of 1-propyl-5-(tetrahydro-2H-pyran-4-ylmethyl)-1H-pyrazole-3-carboxylic acid (4.88 g, 19.3 mmol) and 1-hydroxybenzotriazole (2.87 g, 21.2 mmol) in N,N-dimethylformamide (DMF) (24.4 mL) at room temperature. The mixture was stirred for two hours, cooled in an ice bath, and treated with concentrated ammonium hydroxide (3.9 mL). A precipitate formed, and the mixture was stirred 30 minutes at 0° C. Water (100 mL) was added, and the mixture was stirred for an additional ten minutes. The precipitate was isolated by filtration, washed with water, and dried on the vacuum filter funnel to provide 4.05 g of 1-propyl-5-(tetrahydro-2H-pyran-4-ylmethyl)-1H-pyrazole-3-carboxamide as white crystals.

Aufarbeitung

  1. temperaturecooled in an ice bath
  2. customA precipitate formed
  3. stirringthe mixture was stirred 30 minutes at 0° C
  4. stirringthe mixture was stirred for an additional ten minutes
  5. customThe precipitate was isolated by filtration
  6. washwashed with water
  7. customdried on the vacuum
  8. filtrationfilter funnel

Quellen und Nachweise

ORD-Eintrag
ord-6d08184d45bb454bab2f08f5333c89bf
Quelldatensatz
uspto-grants-2011_05
Patentnummer
US07943636B2

Notizen zur Reaktion

Wird geladen…