HCID 178492681, compound → HCID 178492679, compound

HRID 258672Notes

Reaction equation

HRID 258672 reaction equation
N[C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:19]=1[N:18]=[C:9]([C:10]([NH:12][C:13]1[NH:17][N:16]=[N:15][N:14]=1)=[O:11])[CH:8]=[C:7]2[O:20][CH3:21].COC1C2C(=C([N+]([O-])=O)C=CC=2)N=C(C([NH:29]C2NN=NN=2)=O)C=1>>[NH2:29][C:4]1[CH:5]=[C:6]2[C:19](=[CH:2][CH:3]=1)[N:18]=[C:9]([C:10]([NH:12][C:13]1[NH:17][N:16]=[N:15][N:14]=1)=[O:11])[CH:8]=[C:7]2[O:20][CH3:21]

Participants

3

Reactant 2

HCID 178492681HCID 178492681, compoundHCID 178492682HCID 178492682, compound

Product 1

HCID 178492679HCID 178492679, compound

Procedure

8-Amino-4-methoxy-N(1H-tetrazol- 5-yl)quinaldamide, m.p. 276° (d), was prepared by the hydrogenation of 4-methoxy-8-nitro-N(1H-tetrazol- 5-yl)quinaldamide.

Sources & evidence

ORD record
ord-af98a7ec4e5648b299c3c37fc90a794e
Source dataset
uspto-grants-1977_07
Patent number
US04034075

Reaction notes

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