HCID 21426420, compound → HCID 178522680, compound

HRID 1580054Notes

Reaction equation

HRID 1580054 reaction equation
C([C:5]1[CH:6]=[C:7]2[C:20](=[CH:21][CH:22]=1)[N:19]=[C:10]([C:11]([NH:13][C:14]1[NH:18][N:17]=[N:16][N:15]=1)=[O:12])[CH:9]=[C:8]2[Cl:23])CCC.C(C1C=C2C(=CC=1)N=C(C(Cl)=O)C=C2Cl)CCC.NC1NN=NN=1>>[Cl:23][C:8]1[C:7]2[C:20](=[CH:21][CH:22]=[CH:5][CH:6]=2)[N:19]=[C:10]([C:11]([NH:13][C:14]2[NH:18][N:17]=[N:16][N:15]=2)=[O:12])[CH:9]=1

Participants

4

Reactant 3

HCID 21426420HCID 21426420, compoundHCID 178440677HCID 178440677, compoundHCID 178509299HCID 178509299, compound

Product 1

HCID 178522680HCID 178522680, compound

Procedure

In a similar manner 6-butyl-4-chloro-N-(1H-tetrazol-5-yl)quinaldamide, m.p. 275° was prepared from 6-butyl-4-chloroquinaldoyl chloride and 5 -aminotetrazole.

Sources & evidence

ORD record
ord-5194bcbc399f48a28de801cae156c6bf
Source dataset
uspto-grants-1976_01
Patent number
US03932416

Reaction notes

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