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公开(公告)号:AU2011228146A1
公开(公告)日:2012-10-25
申请号:AU2011228146
申请日:2011-03-15
Applicant: UBE INDUSTRIES
Inventor: KAKITA KAZUAKI , IWASA TAKAFUMI , KAKUTA YOSHIHISA , SHIRAI MASASHI , FURUYA TOSHIO , NISHINO SHIGEYOSHI , SHIMA HIDETAKA
Abstract: Disclosed is a binuclear ruthenium complex dye which has a higher absorption coefficient and exhibits light absorbing power even in a longer wavelength region and which makes it possible to provide a photoelectric conversion element and a photochemical cell that can perform the conversion of sunlight into electricity over a wide wavelength region and with high photoelectric conversion efficiency. Also disclosed is a binuclear ruthenium complex dye which makes it possible to provide a photoelectric conversion element and a photochemical cell that exhibit high durability.
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公开(公告)号:DE602004032028D1
公开(公告)日:2011-05-12
申请号:DE602004032028
申请日:2004-07-30
Applicant: UBE INDUSTRIES
Inventor: NISHINO SHIGEYOSHI , HIROTSU KENJI , SHIMA HIDETAKA , ODA HIROYUKI , SUZUKI SHINOBU
IPC: C07D239/88 , C07C67/31
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公开(公告)号:AT503747T
公开(公告)日:2011-04-15
申请号:AT04748126
申请日:2004-07-30
Applicant: UBE INDUSTRIES
Inventor: NISHINO SHIGEYOSHI , HIROTSU KENJI , SHIMA HIDETAKA , ODA HIROYUKI , SUZUKI SHINOBU
IPC: C07D239/88 , C07C67/31
Abstract: A process comprising a reaction of ethyl 2-amino-4,5-bis(2-methoxyethoxy)benzoate with a formic acid compound in the presence of an ammonium carboxylate gives 6,7-bis(2-methoxyethoxy)quinazolin-4-one in a high yield.
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公开(公告)号:CA2398113C
公开(公告)日:2010-01-05
申请号:CA2398113
申请日:2001-01-24
Applicant: UBE INDUSTRIES , NISSAN CHEMICAL IND LTD
Inventor: NISHINO SHIGEYOSHI , OKADA NAOKO , HARADA KATSUMASA , SHIMA HIDETAKA , HARADA TAKASHI
IPC: C07D215/12 , C07D215/14
Abstract: 3-[2-Cyclopropyl-4-(4-fluorophenyl)-3- quinolyl]prop-2-enenitrile represented by (3) is prepared by reacting 2-cyclopropyl-4-(4-fluorophenyl)quinoline-3- carbaldehyde represented by (1) with acetonitrile in the presence of a base and then adding a dehydrating to the reaction mixture to conduct dehydration. Under ordinary conditions, novel 3-[2-cyclopropyl-4-(4-fluorophenyl)- quinolin-3-yl]-3-hydroxypropionitrile represented by (2) is formed as an intermediate in the above reaction. Incidentally, when the above reaction is conducted in an organic solvent, 3-[2-cyclopropyl-4-(4-fluorophenyl)-3- quinolyl]-prop-2-enenitrile is directly formed. (see formula 1) (see formula 2) (see formula 3)
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公开(公告)号:CA2398138C
公开(公告)日:2009-12-22
申请号:CA2398138
申请日:2001-01-24
Applicant: NISSAN CHEMICAL IND LTD , UBE INDUSTRIES
Inventor: SHIMA HIDETAKA , HARADA TAKASHI , HARADA KATSUMASA , NISHINO SHIGEYOSHI , OKADA NAOKO
IPC: C07D215/14 , C07B61/00
Abstract: 3-[2-Cyclopropyl-4-(4-fluorophenyl)-3- quinolyl]prop-2-enal of the below formula (see above formula) is prepared in a high yield by reducing 3-[2-cyclopropyl-4- (4-fluorophenyl)-3-quinolyl]prop-2-enenitrile with Raney nickel either in the presence of formic acid and 0.25 to 1 part by volume of water per part by volume of formic acid or in the presence of both an amine salt of formic acid and an organic acid.
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公开(公告)号:DE60317519D1
公开(公告)日:2007-12-27
申请号:DE60317519
申请日:2003-06-10
Applicant: UBE INDUSTRIES
Inventor: NISHINO SHIGEYOSHI , HIROTSU KENJI , SHIMA HIDETAKA , SUZUKI SHINOBU
IPC: C07D309/12
Abstract: The present invention relates to a process for preparing tetrahydropyran-4-ol which comprises the steps of (A) a cyclization step of preparing tetrahydropyranyl-4-formate represented by the formula (1): by reacting 3-buten-1-ol, a formaldehyde compound and formic acid, and (B) then, a solvolysis step of subjecting the tetrahydropyranyl-4-formate to solvolysis to obtain tetrahydropyran-4-ol represented by the formula (2): and an intermediate and a process for preparing the same.
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27.
公开(公告)号:AU2003242216A1
公开(公告)日:2003-12-22
申请号:AU2003242216
申请日:2003-06-10
Applicant: UBE INDUSTRIES
Inventor: SHIMA HIDETAKA , SUZUKI SHINOBU , NISHINO SHIGEYOSHI , HIROTSU KENJI
IPC: C07D309/12
Abstract: The present invention relates to a process for preparing tetrahydropyran-4-ol which comprises the steps of (A) a cyclization step of preparing tetrahydropyranyl-4-formate represented by the formula (1): by reacting 3-buten-1-ol, a formaldehyde compound and formic acid, and (B) then, a solvolysis step of subjecting the tetrahydropyranyl-4-formate to solvolysis to obtain tetrahydropyran-4-ol represented by the formula (2): and an intermediate and a process for preparing the same.
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28.
公开(公告)号:HK1054024A1
公开(公告)日:2003-11-14
申请号:HK03106190
申请日:2003-08-29
Applicant: UBE INDUSTRIES
Inventor: HARADA KATSUMASA , NISHINO SHIGEYOSHI , SHIMA HIDETAKA , HIROTSU KENJI , NISHIMURA MINORU
IPC: C07D309/08 , C07D309/14 , C07D
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公开(公告)号:AU2003207291A1
公开(公告)日:2003-09-02
申请号:AU2003207291
申请日:2003-02-06
Applicant: UBE INDUSTRIES
Inventor: HARADA TAKASHI , ODA HIROYUKI , NISHINO SHIGEYOSHI , HIROTSU KENJI , SHIMA HIDETAKA
IPC: C07D239/88 , C07D239/94 , C07D239/86
Abstract: Preparation of an optionally substituted 4-aminoquinazoline compound (III) involves: (i) reacting the corresponding quinazolin-4-one compound (I) with a chlorinating agent in a first organic solvent in the presence of an organic base; and (ii) reacting the product with ammonia or amine (II) in a second organic solvent. Preparation of a 4-aminoquinazoline compound of formula (III) involves: (i) reacting a quinazolin-4-one compound of formula (I) with a chlorinating agent in a first organic solvent in the presence of an organic base; and (ii) reacting the product with ammonia or amine of formula R 5>NHR 6>(II) in a second organic solvent. [Image] R 1>-R 4>group which is inert in the reaction conditions; and R 5>, R 6>H or substituent. An independent claim is also included for the preparation of 6-halo-4-chloroquinazoline of formula (VII) from 6-halo-quinazolin-4-one of formula (VI). [Image] X : halo; and Ar' : optionally substituted aryl.
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公开(公告)号:AU2710001A
公开(公告)日:2001-07-31
申请号:AU2710001
申请日:2001-01-24
Applicant: UBE INDUSTRIES , NISSAN CHEMICAL IND LTD
Inventor: HARADA KATSUMASA , NISHINO SHIGEYOSHI , SHIMA HIDETAKA , HARADA TAKASHI , OKADA NAOKO
IPC: C07D215/14 , C07B61/00
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