JP2018099880A5 - - Google Patents

Info

Publication number

JP2018099880A5

JP2018099880A5 JP2017213857A JP2017213857A JP2018099880A5 JP 2018099880 A5 JP2018099880 A5 JP 2018099880A5 JP 2017213857 A JP2017213857 A JP 2017213857A JP 2017213857 A JP2017213857 A JP 2017213857A JP 2018099880 A5 JP2018099880 A5 JP 2018099880A5

Authority

JP

Japan

Prior art keywords

group

substituted

unsubstituted aryl

alkyl group

formula

Prior art date

2017-11-06

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

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• 239000000975 dye Substances 0.000 claims description 25
• 239000000463 material Substances 0.000 claims description 15
• 150000001875 compounds Chemical class 0.000 claims description 13
• AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 claims description 11
• 239000001043 yellow dye Substances 0.000 claims description 11
• 125000000217 alkyl group Chemical group 0.000 claims 43
• 125000003118 aryl group Chemical group 0.000 claims 37
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 23
• 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 6
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 5
• 125000002252 acyl group Chemical group 0.000 claims 4
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
• 125000001424 substituent group Chemical group 0.000 claims 3
• 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 2
• 125000003277 amino group Chemical group 0.000 claims 2
• 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 2
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 2
• 125000004093 cyano group Chemical group *C#N 0.000 claims 2
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 2
• 125000005843 halogen group Chemical group 0.000 claims 2
• 125000005010 perfluoroalkyl group Chemical group 0.000 claims 2
• NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 claims 1
• 125000002947 alkylene group Chemical group 0.000 claims 1
• 150000001450 anions Chemical class 0.000 claims 1
• 125000001624 naphthyl group Chemical group 0.000 claims 1
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
• 0 *C(NC(C(C(Cl)=C1*)=O)=CC1=Nc(c(*)c1)ccc1N(*)*)=O Chemical compound *C(NC(C(C(Cl)=C1*)=O)=CC1=Nc(c(*)c1)ccc1N(*)*)=O 0.000 description 2
• 238000004040 coloring Methods 0.000 description 1
• 238000000034 method Methods 0.000 description 1
• 230000003287 optical effect Effects 0.000 description 1