JP2014506374A5 - - Google Patents

Info

Publication number

JP2014506374A5

JP2014506374A5 JP2013542387A JP2013542387A JP2014506374A5 JP 2014506374 A5 JP2014506374 A5 JP 2014506374A5 JP 2013542387 A JP2013542387 A JP 2013542387A JP 2013542387 A JP2013542387 A JP 2013542387A JP 2014506374 A5 JP2014506374 A5 JP 2014506374A5

Authority

JP

Japan

Prior art keywords

atoms

substituted

linear

branched

aryl

Prior art date

2011-11-09

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.)

Granted

Links

• Espacenet
• Global Dossier
• Discuss

• 125000004432 carbon atom Chemical group C* 0.000 claims description 89
• 125000003118 aryl group Chemical group 0.000 claims description 33
• 125000000217 alkyl group Chemical group 0.000 claims description 27
• 125000001072 heteroaryl group Chemical group 0.000 claims description 18
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 14
• 125000003545 alkoxy group Chemical group 0.000 claims description 12
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 9
• 239000000654 additive Substances 0.000 claims description 5
• 125000004430 oxygen atom Chemical group O* 0.000 claims description 5
• 125000003342 alkenyl group Chemical group 0.000 claims description 4
• 125000004663 dialkyl amino group Chemical group 0.000 claims description 4
• 125000004414 alkyl thio group Chemical group 0.000 claims description 3
• 125000005110 aryl thio group Chemical group 0.000 claims description 3
• 125000004104 aryloxy group Chemical group 0.000 claims description 3
• 150000001875 compounds Chemical class 0.000 claims description 3
• 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 3
• 230000000996 additive effect Effects 0.000 claims description 2
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
• 125000003282 alkyl amino group Chemical group 0.000 claims 1
• 239000003792 electrolyte Substances 0.000 description 4
• 238000009472 formulation Methods 0.000 description 4
• 239000000203 mixture Substances 0.000 description 4
• 238000006243 chemical reaction Methods 0.000 description 2
• -1 methoxyphenylmethyl Chemical group 0.000 description 2
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
• UUIMDJFBHNDZOW-UHFFFAOYSA-N 2-tert-butylpyridine Chemical compound CC(C)(C)C1=CC=CC=N1 UUIMDJFBHNDZOW-UHFFFAOYSA-N 0.000 description 1
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
• 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
• 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
• 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1