1,2-Dichloroethane → N-{1-[Amino(oxo)acetyl]pentyl}-2-(4-phenyl-1H-pyrazol-1-yl)nicotinamide

HRID 12429

Reaction equation

HRID 12429 reaction equation
C(Cl)CCl.ClC(Cl)C(O)=O.[NH2:11][C:12](=[O:40])[CH:13]([CH:15]([NH:20][C:21]([C:23]1[C:24]([N:29]2[CH:33]=[C:32]([C:34]3[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=3)[CH:31]=[N:30]2)=[N:25][CH:26]=[CH:27][CH:28]=1)=[O:22])[CH2:16][CH2:17][CH2:18][CH3:19])[OH:14].O>CS(C)=O>[NH2:11][C:12](=[O:40])[C:13]([CH:15]([NH:20][C:21](=[O:22])[C:23]1[CH:28]=[CH:27][CH:26]=[N:25][C:24]=1[N:29]1[CH:33]=[C:32]([C:34]2[CH:35]=[CH:36][CH:37]=[CH:38][CH:39]=2)[CH:31]=[N:30]1)[CH2:16][CH2:17][CH2:18][CH3:19])=[O:14]

Participants

6

Procedure

0.47 g of EDC and 0.08 ml of dichloroacetic acid were added to 100 mg of N-[1-(2-amino-1-hydroxy-2-oxoethyl)pentyl]-2-(4-phenyl-1H-pyrazol-1-yl)pyridine-3-carboxamide (0.25 mmol) in 4 ml of dimethyl sulfoxide, and the mixture was stirred at room temperature overnight. For workup, the reaction mixture was poured into H2O, and the resulting precipitate was filtered off with suction and dried in a vacuum drying oven at 40° C. 77 mg of the title compound were obtained as an amorphous white solid.

Workup

  1. filtrationthe resulting precipitate was filtered off with suction
  2. customdried in a vacuum
  3. customdrying oven at 40° C

Sources & evidence

ORD record
ord-9e84da6c8ed8414fa732e854834986ac
Source dataset
uspto-grants-2010_06
Patent number
US07728012B2

Linked notes

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