GB1414155A - Triazole derivatives - Google Patents

Info

Publication number

GB1414155A

GB1414155A GB5293072A GB5293072A GB1414155A GB 1414155 A GB1414155 A GB 1414155A GB 5293072 A GB5293072 A GB 5293072A GB 5293072 A GB5293072 A GB 5293072A GB 1414155 A GB1414155 A GB 1414155A

Authority

GB

United Kingdom

Prior art keywords

group

hydrogen atom

cyano

conh

optionally substituted

Prior art date

1971-11-19

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Expired

Links

• Espacenet
• Global Dossier
• Discuss

• 229940042055 systemic antimycotics triazole derivative Drugs 0.000 title abstract 3
• 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 8
• 150000001875 compounds Chemical class 0.000 abstract 3
• NQMUGNMMFTYOHK-UHFFFAOYSA-N 1-methoxynaphthalene Chemical compound C1=CC=C2C(OC)=CC=CC2=C1 NQMUGNMMFTYOHK-UHFFFAOYSA-N 0.000 abstract 2
• PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 abstract 2
• UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 2
• 125000003118 aryl group Chemical group 0.000 abstract 2
• 238000005282 brightening Methods 0.000 abstract 2
• 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
• ZZQUMSVZBTVNGH-UHFFFAOYSA-N 2-(4-methylphenyl)benzo[e]benzotriazole Chemical compound C1=CC(C)=CC=C1N1N=C2C3=CC=CC=C3C=CC2=N1 ZZQUMSVZBTVNGH-UHFFFAOYSA-N 0.000 abstract 1
• XOSDYLFXPMFRGF-UHFFFAOYSA-N 2-methyl-5-nitrobenzonitrile Chemical compound CC1=CC=C([N+]([O-])=O)C=C1C#N XOSDYLFXPMFRGF-UHFFFAOYSA-N 0.000 abstract 1
• IHJPDCGKQAXUEX-UHFFFAOYSA-N 4-(4-formyltriazol-2-yl)benzonitrile Chemical compound N1=C(C=O)C=NN1C1=CC=C(C#N)C=C1 IHJPDCGKQAXUEX-UHFFFAOYSA-N 0.000 abstract 1
• SHFOPZVVFLRCJM-UHFFFAOYSA-N 5-benzo[e]benzotriazol-2-yl-2-methylbenzonitrile Chemical compound C1=C(C#N)C(C)=CC=C1N1N=C2C3=CC=CC=C3C=CC2=N1 SHFOPZVVFLRCJM-UHFFFAOYSA-N 0.000 abstract 1
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
• 125000004062 acenaphthenyl group Chemical group C1(CC2=CC=CC3=CC=CC1=C23)* 0.000 abstract 1
• 125000003172 aldehyde group Chemical group 0.000 abstract 1
• 125000000217 alkyl group Chemical group 0.000 abstract 1
• 150000001450 anions Chemical group 0.000 abstract 1
• OGBVRMYSNSKIEF-UHFFFAOYSA-L benzyl-dioxido-oxo-$l^{5}-phosphane Chemical compound [O-]P([O-])(=O)CC1=CC=CC=C1 OGBVRMYSNSKIEF-UHFFFAOYSA-L 0.000 abstract 1
• 125000004432 carbon atom Chemical group C* 0.000 abstract 1
• 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
• 125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 abstract 1
• 239000003795 chemical substances by application Substances 0.000 abstract 1
• -1 cyano, carboxyl Chemical group 0.000 abstract 1
• 229910052739 hydrogen Inorganic materials 0.000 abstract 1
• 239000001257 hydrogen Substances 0.000 abstract 1
• 239000000463 material Substances 0.000 abstract 1
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
• 150000002828 nitro derivatives Chemical class 0.000 abstract 1
• 230000003287 optical effect Effects 0.000 abstract 1
• BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 abstract 1