HCID 178420081, compound → HCID 178420707, compound

HRID 2074022Notes

Reaction equation

HRID 2074022 reaction equation
N1C2C(=CC=CC=2)C=CC=1COC1C=C(C=CC=1)OCC1C=C(C2NN=NN=2)C=CC=1.N1C2C(=CC=CC=2)C=CC=1COC1C=C(CC2C=CC=CC=2CC2NN=NN=2)C=CC=1.[N:63]1[C:72]2[C:67](=[CH:68][CH:69]=[CH:70][CH:71]=2)[CH:66]=[CH:65][C:64]=1[CH2:73][O:74][C:75]1[CH:76]=[C:77]([CH:92]=[CH:93][CH:94]=1)[O:78][CH2:79][C:80]1C=[C:82]([CH:89]=[CH:90][CH:91]=1)[CH2:83][C:84]1[NH:88][N:87]=[N:86][N:85]=1.N1C2C(=CC=CC=2)C=CC=1COC1C=C(C=CC=1)OCC1C=CC(CC2NN=NN=2)=CC=1>>[N:63]1[C:72]2[C:67](=[CH:68][CH:69]=[CH:70][CH:71]=2)[CH:66]=[CH:65][C:64]=1[CH2:73][O:74][C:75]1[CH:76]=[C:77]([CH:92]=[CH:93][CH:94]=1)[O:78][CH2:79][C:80]1[CH:91]=[CH:90][CH:89]=[CH:82][C:83]=1[C:84]1[NH:88][N:87]=[N:86][N:85]=1

Participants

5

Reactant 4

HCID 178420081HCID 178420081, compoundHCID 178420506HCID 178420506, compoundHCID 178420711HCID 178420711, compoundHCID 178420712HCID 178420712, compound

Product 1

HCID 178420707HCID 178420707, compound

Procedure

(M.P. 166°-170° C.), 5-(3-(3-(2-quinolinylmethyloxy)phenoxymethyl)phenyl)tetrazole (M.P. 155° C. dec.), 5-(2-(3-(2-quinolinylmethyloxy)phenylmethyl)benzyl tetrazole (M.P. 145.5°-147° C.), 5-(3-(3-(2-quinolinylmethyloxy)phenoxymethyl)benzyl tetrazole (M.P. 161°-164° C.), or 5-(4-(3-(2-quinolinylmethyloxy)phenoxymethyl)benzyl tetrazole (M.P. 149°-152° C.).

Sources & evidence

ORD record
ord-51f4836969b84a57a539947559942ca1
Source dataset
uspto-grants-1990_04
Patent number
US04920132

Reaction notes

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