HCID 13373708, compound → 92616-43-8

HRID 1981824Notes

Reaction equation

HRID 1981824 reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([NH2:8])[N:5]=[C:4]([C:9]2[CH:18]=[CH:17][C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[C:10]=2[O:19]C)[N:3]=1.NC1N=C(N)N=[C:24]([C:29]2[CH:38]=[CH:37][C:36]3C(=CC=CC=3)[C:30]=2[O:39]CC2C=CC=CC=2)[N:23]=1>>[NH2:1][C:2]1[N:7]=[C:6]([NH:8][C:30](=[O:39])[C:29]2[CH:38]=[CH:37][CH:36]=[N:23][CH:24]=2)[N:5]=[C:4]([C:9]2[CH:18]=[CH:17][C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[C:10]=2[OH:19])[N:3]=1

Participants

3

Reactant 2

HCID 13373708HCID 13373708, compoundHCID 13373712HCID 13373712, compound

Product 1

HCID 13566764892616-43-8

Procedure

The same methods as in the preceding examples were conducted using 2,4-diamino-6-(1-methoxy-2-naphthyl)-s-triazine or 2,4-diamino-6-(1-benzyloxy-2-naphthyl)-s-triazine to afford 2-amino-4-nicotinamido-6-(1-hydroxy-2-naphthyl)-s-triazine, pale yellow needles, melting point 301° to 302° C.

Sources & evidence

ORD record
ord-88fd74b38d294911bda726f7139b2fb8
Source dataset
uspto-grants-1986_06
Patent number
US04593025

Reaction notes

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