Hydrochloric Acid → 2-Amino-4-nicotinamido-6-phenyl-s-triazine

HRID 866406

Reaction equation

HRID 866406 reaction equation
[CH:1]1[CH:2]=[CH:3][C:4]([C:7]2[N:8]=[C:9]([NH2:14])[N:10]=[C:11]([NH2:13])[N:12]=2)=[CH:5][CH:6]=1.[C:15](Cl)(=[O:22])[C:16]1[CH:21]=[CH:20][CH:19]=[N:18][CH:17]=1.Cl>N1C=CC=CC=1>[NH2:13][C:11]1[N:10]=[C:9]([NH:14][C:15](=[O:22])[C:16]2[CH:21]=[CH:20][CH:19]=[N:18][CH:17]=2)[N:8]=[C:7]([C:4]2[CH:3]=[CH:2][CH:1]=[CH:6][CH:5]=2)[N:12]=1.[C:15]([NH:13][C:11]1[N:10]=[C:9]([NH:14][C:15](=[O:22])[C:16]2[CH:21]=[CH:20][CH:19]=[N:18][CH:17]=2)[N:8]=[C:7]([C:4]2[CH:3]=[CH:2][CH:1]=[CH:6][CH:5]=2)[N:12]=1)(=[O:22])[C:16]1[CH:21]=[CH:20][CH:19]=[N:18][CH:17]=1

Participants

6

Conditions

Temperature
60 °C

Procedure

1.9 g of benzoguanamine and 3.6 g of nicotinic acid chloride (or an equivalent amount of the hydrochloride) are dissolved in 70 ml of pyridine and heated at 60° C for 6 hours. The reaction mixture is processed as described in Example 4 to yield 0.17 g of 2-amino-4-nicotinamido-6-phenyl-s-triazine [mononicotinoylbenzoguanamine] and 1.2 g of 2,4-bis(nicotinamido)-6-phenyl-s-triazine [dinicotinoylbenzoguanamine].

Sources & evidence

ORD record
ord-181783f4f177426eb5afa527626475a3
Source dataset
uspto-grants-1978_07
Patent number
US04098892

Linked notes

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