JP2008514617A5 - - Google Patents
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- JP2008514617A5 JP2008514617A5 JP2007533651A JP2007533651A JP2008514617A5 JP 2008514617 A5 JP2008514617 A5 JP 2008514617A5 JP 2007533651 A JP2007533651 A JP 2007533651A JP 2007533651 A JP2007533651 A JP 2007533651A JP 2008514617 A5 JP2008514617 A5 JP 2008514617A5
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- Japan
- Prior art keywords
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- compound according
- compound
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- substituted
- Prior art date
- 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
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- 150000001875 compounds Chemical class 0.000 claims description 21
- 125000003118 aryl group Chemical group 0.000 claims description 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- 125000005157 alkyl carboxy group Chemical group 0.000 claims description 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 125000001624 naphthyl group Chemical group 0.000 claims description 3
- 125000004434 sulfur atom Chemical group 0.000 claims description 3
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 2
- 239000000047 product Substances 0.000 claims 5
- FECNOIODIVNEKI-UHFFFAOYSA-N 2-[(2-aminobenzoyl)amino]benzoic acid Chemical compound NC1=CC=CC=C1C(=O)NC1=CC=CC=C1C(O)=O FECNOIODIVNEKI-UHFFFAOYSA-N 0.000 claims 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- 239000000376 reactant Substances 0.000 claims 3
- 238000006243 chemical reaction Methods 0.000 claims 2
- ZYHQGITXIJDDKC-UHFFFAOYSA-N 2-[2-(2-aminophenyl)ethyl]aniline Chemical group NC1=CC=CC=C1CCC1=CC=CC=C1N ZYHQGITXIJDDKC-UHFFFAOYSA-N 0.000 claims 1
- GZOJTRITAZODJV-UHFFFAOYSA-N 3,1-benzoxazin-2-one Chemical compound C1=CC=CC2=COC(=O)N=C21 GZOJTRITAZODJV-UHFFFAOYSA-N 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 239000012024 dehydrating agents Substances 0.000 claims 1
- 230000018044 dehydration Effects 0.000 claims 1
- 238000006297 dehydration reaction Methods 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 238000010992 reflux Methods 0.000 claims 1
- 238000006798 ring closing metathesis reaction Methods 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 description 6
- 125000004448 alkyl carbonyl group Chemical group 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 125000004093 cyano group Chemical group *C#N 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 125000005907 alkyl ester group Chemical group 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- 125000001188 haloalkyl group Chemical group 0.000 description 2
- 125000001475 halogen functional group Chemical group 0.000 description 2
- -1 methoxy, butyl Chemical group 0.000 description 2
- 0 CC(NC(*)(*)*)=* Chemical compound CC(NC(*)(*)*)=* 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 238000000295 emission spectrum Methods 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 229910052717 sulfur Chemical group 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/949,075 US7192471B2 (en) | 2004-09-24 | 2004-09-24 | Aryl-ureido benzoxazinone compounds |
| US10/949,075 | 2004-09-24 | ||
| PCT/US2005/034155 WO2006036790A1 (en) | 2004-09-24 | 2005-09-22 | Aryl-ureido benzoxazinone compounds |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008514617A JP2008514617A (ja) | 2008-05-08 |
| JP2008514617A5 true JP2008514617A5 (enExample) | 2012-03-22 |
| JP5014996B2 JP5014996B2 (ja) | 2012-08-29 |
Family
ID=35414944
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007533651A Expired - Fee Related JP5014996B2 (ja) | 2004-09-24 | 2005-09-22 | アリールウレイドベンゾキサジノン化合物 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US7192471B2 (enExample) |
| EP (1) | EP1794136B1 (enExample) |
| JP (1) | JP5014996B2 (enExample) |
| KR (1) | KR20070055600A (enExample) |
| CN (1) | CN100569759C (enExample) |
| AT (1) | ATE439353T1 (enExample) |
| DE (1) | DE602005015989D1 (enExample) |
| ES (1) | ES2329266T3 (enExample) |
| WO (1) | WO2006036790A1 (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7892386B2 (en) * | 2007-08-24 | 2011-02-22 | Dymax Corporation | Radiation-curable fluorescing compositions |
| US7740693B2 (en) | 2007-10-01 | 2010-06-22 | Honeywell International Inc. | Organic fluorescent sulfonyl ureido benzoxazinone pigments |
| WO2011039199A1 (en) * | 2009-09-30 | 2011-04-07 | D W Spinks (Embossing) Limited | A security feature for inclusion in a security paper |
| DE102010063012B4 (de) | 2010-12-14 | 2018-10-18 | Bundesdruckerei Gmbh | Aktivierbares Sicherheitselement |
| CN103328453B (zh) * | 2011-01-13 | 2015-10-07 | 巴斯夫欧洲公司 | 荧光化合物 |
| US11873432B2 (en) * | 2018-11-29 | 2024-01-16 | Honeywell International Inc. | Luminescent materials including a luminescent benzothiazole, articles including a security feature, and methods of forming luminescent particles including a luminescent benzothiazole |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3335137A (en) * | 1964-11-17 | 1967-08-08 | Vnii Khim Reaktivov I Osobo Ch | Process of manufacturing substituted 2-(21-arylsulphonyl aminophenyl)-4h, 3, 1-benzoxazin-4-ones |
| US3740402A (en) * | 1971-03-01 | 1973-06-19 | American Cyanamid Co | Certain 2-(0-sulfonamidophenyl)-4(3h)-quinazolinones |
| US3892972A (en) * | 1971-03-01 | 1975-07-01 | American Cyanamid Co | Method of producing a luminescent surface containing substituted sulfonamido and carboxamido phenyl quinazolones |
| US4657893A (en) * | 1984-05-09 | 1987-04-14 | Syntex (U.S.A.) Inc. | 4H-3,1-benzoxazin-4-ones and related compounds and use as enzyme inhibitors |
| DE3514183A1 (de) * | 1985-04-19 | 1986-10-23 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung substituierter 2-phenyl-4h-3,1-benzoxazin-4-one |
| US4745116A (en) * | 1985-06-25 | 1988-05-17 | Syntex (U.S.A.) Inc. | 2-oxy-4H-3,1-benzoxazin-4-ones and related compounds and pharmaceutical use |
| GB8724570D0 (en) | 1987-10-20 | 1987-11-25 | De La Rue Thomas & Co Ltd | Fluorescent compounds |
| JP3479358B2 (ja) * | 1994-08-08 | 2003-12-15 | アヴェンティス・リサーチ・ウント・テクノロジーズ・ゲーエムベーハー・ウント・コー・カーゲー | 有機エレクトロルミネッセンス素子 |
| US5652237A (en) * | 1994-09-09 | 1997-07-29 | Warner-Lambert Company | 2-substituted-4H-3, 1-benzoxazin-4-ones and benzthiazin-4-ones as inhibitors of complement C1r protease for the treatment of inflammatory processes |
| FR2730499B1 (fr) * | 1995-02-14 | 2004-02-27 | Imaje Sa | Composition d'encre pour le marquage et l'authentification d'objets |
| US5985872A (en) * | 1995-05-24 | 1999-11-16 | G.D. Searle & Co. | 2-amino-benzoxazinones for the treatment of viral infections |
| JP3358056B2 (ja) * | 1998-10-16 | 2002-12-16 | 日本製紙株式会社 | 感熱記録体 |
| US6806269B1 (en) * | 1999-07-12 | 2004-10-19 | G. D. Searle & Cop | 2-Amino-benzoxazinones for the treatment of herpes simplex virus |
| CA2424300A1 (en) * | 2000-10-02 | 2002-04-11 | Molecular Probes, Inc. | Reagents for labeling biomolecules having aldehyde or ketone moieties |
| WO2002085868A1 (en) * | 2001-04-23 | 2002-10-31 | Astrazeneca Ab | Benzoxazinone derivatives for use in the treatment of angiogenesis |
| US20040116420A1 (en) * | 2001-06-13 | 2004-06-17 | Wataru Takahashi | Remedial agent for viral infectious disease |
| CA2454080A1 (en) * | 2001-08-13 | 2003-02-27 | Robert Edward Detlefsen | Ultraviolet light absorbers |
| JP4266542B2 (ja) | 2001-08-31 | 2009-05-20 | オリヱント化学工業株式会社 | 青色発光性インキ組成物 |
| US6774232B2 (en) * | 2001-10-22 | 2004-08-10 | Cytec Technology Corp. | Low color, low sodium benzoxazinone UV absorbers and process for making same |
| US20040219390A1 (en) * | 2003-01-23 | 2004-11-04 | Honeywell International, Inc. | Benzoxazinone and quinazolinone derivatives |
-
2004
- 2004-09-24 US US10/949,075 patent/US7192471B2/en not_active Expired - Lifetime
-
2005
- 2005-09-22 EP EP05798292A patent/EP1794136B1/en not_active Expired - Lifetime
- 2005-09-22 WO PCT/US2005/034155 patent/WO2006036790A1/en not_active Ceased
- 2005-09-22 KR KR1020077008638A patent/KR20070055600A/ko not_active Withdrawn
- 2005-09-22 DE DE602005015989T patent/DE602005015989D1/de not_active Expired - Lifetime
- 2005-09-22 ES ES05798292T patent/ES2329266T3/es not_active Expired - Lifetime
- 2005-09-22 JP JP2007533651A patent/JP5014996B2/ja not_active Expired - Fee Related
- 2005-09-22 AT AT05798292T patent/ATE439353T1/de not_active IP Right Cessation
- 2005-09-22 CN CNB2005800398785A patent/CN100569759C/zh not_active Expired - Fee Related
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