2-Pyrazinecarboxylic acid → HCID 23326136, compound

HRID 1380265Notes

Reaction equation

HRID 1380265 reaction equation
[N:1]1[CH:6]=[CH:5][N:4]=[CH:3][C:2]=1[C:7]([OH:9])=O.[CH2:10]([NH:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH:26]([CH3:28])[CH3:27])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH:16]([CH3:18])[CH3:17]>>[CH2:10]([N:19]([CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH:26]([CH3:28])[CH3:27])[C:7]([C:2]1[CH:3]=[N:4][CH:5]=[CH:6][N:1]=1)=[O:9])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH:16]([CH3:17])[CH3:18]

Participants

3

Reactant 2

HCID 10472-Pyrazinecarboxylic acidHCID 168808Isononanamine, N-isononyl-

Product 1

HCID 23326136HCID 23326136, compound

Procedure

N,N-diisononylpyrazine-2-carboxamide was prepared from pyrazine-2-carboxylic acid and commercial di-isononylamine using the general method of Example 11. The product had a boiling range of 163°-165° C. at 0.15 mm of mercury pressure.

Sources & evidence

ORD record
ord-1a635084d16e4c00b5248ccf13afe273
Source dataset
uspto-grants-1986_04
Patent number
US04581220

Reaction notes

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