专利检索 ipc:"C07C327/40" 第 1 页

1.

发明专利
Substituted benzenesulfonyl ureas and - thioureas, a medicament for use and containing their pharmaceutical formulations based on the preparation and these compounds 失效

公开(公告)号：JP3905573B2

公开(公告)日：2007-04-18

申请号：JP5263396

申请日：1996-02-16

申请人： ヘキスト・ゲゼルシャフト・ミト・ベシュレンクテル・ハフツング

发明人： ウーヴエ・ゲルラハ , デイーター・マニア , ハインツ・ゲーゲライン , ハインリヒ・エングラート , ヨーアヒム・カイザー

IPC分类号： A61K31/18 , C07C311/58 , A61K31/64 , A61P9/00 , A61P9/04 , A61P9/06 , A61P9/10 , C07C233/00 , C07C303/36 , C07C303/40 , C07C311/57 , C07C311/59 , C07C327/40 , C07C335/00 , C07C335/42

CPC分类号： C07C335/42 , C07C311/58 , C07C2601/02 , C07C2601/14 , Y10S514/821

2.

发明专利
失效

公开(公告)号：JP2836215B2

公开(公告)日：1998-12-14

申请号：JP20124390

申请日：1990-07-31

申请人： NIPPON SOODA KK

发明人： ISHIMITSU KEIICHI , SUZUKI JUNJI , OOISHI HARUHITO , YAMADA TOMIO , HATANO RENPEI , TAKAKUSA NOBUO

IPC分类号： C07D237/08 , A01N37/52 , A01N43/40 , A01N43/54 , A01N43/58 , A01N43/60 , A01N43/78 , A01N43/84 , A01N47/02 , C07C249/02 , C07C249/12 , C07C251/08 , C07C251/12 , C07C251/18 , C07C251/24 , C07C251/38 , C07C251/42 , C07C251/48 , C07C257/00 , C07C257/14 , C07C259/00 , C07C259/14 , C07C327/40 , C07D213/53 , C07D213/60 , C07D239/26 , C07D241/12 , C07D241/16 , C07D277/20 , C07D277/28 , C07D277/32 , C07D409/12 , C07D413/12

3.

发明专利
PRODUCTION OF FLUORINE-CONTAINING COMPOUND 失效

公开(公告)号：JPH10287596A

公开(公告)日：1998-10-27

申请号：JP14249897

申请日：1997-05-30

申请人： SAGAMI CHEM RES

发明人： FUCHIGAMI TAKAMASA , HAGIWARA TOSHINORI

IPC分类号： A61K31/40 , A61K31/02 , A61K31/075 , A61K31/215 , A61K31/23 , A61K31/26 , A61K31/403 , A61K31/4035 , A61P35/00 , C07C17/093 , C07C19/10 , C07C19/14 , C07C41/16 , C07C43/12 , C07C67/11 , C07C69/62 , C07C247/04 , C07C253/30 , C07C255/19 , C07C327/40 , C07C331/04 , C07D209/48

摘要： PROBLEM TO BE SOLVED: To simply obtain a fluorine-containing compound by reacting an α- perfluoroalkylated alcohol with a Broensted acid in an aprotic solvent. SOLUTION: A perfluoroalkylsulfonic acid ester or perfluoroarylsulfonic acid ester of an α-perfluoroalkylated alcohol of the formula R R Rf C-OSO2 Rf [R and R are each H, an alkyl, an aromatic, an aralkyl, an alkenyl or an alkynyl or R and R together may form a ring; Rf and Rf are each a perfluoroalkyl or a perfluoro aromatic] is reacted with a Broensted acid of the formula M m Q n [M is a metal ion or polyatomic cation; Q is a conjugated base of the Broensted acid QHy ; (x), (y), (m) and (n) are each an integer satisfying the formula xm=yn] in a solvent such as DMF at -100 to 200 deg.C to provide the objective fluorine-containing compound of the formula (R R Rf C-)y Q (Q is a Broensted acid residue). The compound can be utilized as a synthetic intermediate for medicines and agrochemicals such as aticancer agents and enzyme inhibitors and functional materials such as ferroelectric liquid crystals.

4.

发明专利
DIHALOPROPENE COMPOUND, INSECTICIDE CONTAINING THE SAME COMPOUND AS ACTIVE INGREDIENT AND ITS PRODUCING INTERMEDIATE 失效

公开(公告)号：JPH09249610A

公开(公告)日：1997-09-22

申请号：JP8404596

申请日：1996-04-05

申请人： SUMITOMO CHEMICAL CO

发明人： MATSUO SANSHIRO , HIROSE TARO , IZUMI KEIICHI , SUZUKI MASAYA , SAKAMOTO NORIYASU , TSUSHIMA KAZUHIRO , SAITO SHIGERU , TAKANO JINKO

IPC分类号： C07D295/18 , A01N31/00 , C07C49/255 , C07C49/577 , C07C49/84 , C07C233/18 , C07C233/20 , C07C235/04 , C07C237/04 , C07C271/10 , C07C271/30 , C07C271/40 , C07C275/04 , C07C275/26 , C07C275/28 , C07C311/02 , C07C311/04 , C07C311/05 , C07C311/23 , C07C311/31 , C07C323/20 , C07C323/31 , C07C323/39 , C07C323/50 , C07C323/64 , C07C325/02 , C07C327/40 , C07C333/04 , C07C335/08 , C07C335/10 , C07D207/16 , C07D207/34 , C07D209/34 , C07D213/79 , C07D237/04 , C07D241/14 , C07D277/20 , C07D277/44 , C07D307/68 , C07D309/28 , C07D319/20 , C07D333/38

摘要： PROBLEM TO BE SOLVED: To obtain a dihalopropene compound having insecticidal activity and useful as an excellent insecticide. SOLUTION: This dihalopropene compound is represented by formula I [R1 is a 1-10C alkyl, etc.; R2 , R3 and R4 are each independently a halogen, a 1-3C haloalkyl, etc.; R5 , R6 and R7 are each independently H, trifluoromethyl, etc.; L is C=W, etc.; X is each independently Cl, Br, etc.; Y is O, NH, etc.; Z is O, S, etc.; (m) is an integer of 0-4; (n) is an integer of 0-2], e.g. 3,5-dichloro-4-(3- aminopropyloxy)-1-(3,3-dichloro-2-propenyloxy)benzene. The compound represented by formula I is obtained by reacting a compound represented by formula II with a compound represented by the formula L2 -CHX2 CH=CX2 (L2 is a halogen, mesyloxy or toluoxy) in the presence of a base (e.g. lithium hydroxide) in an inert solvent (e.g. acetone).

5.

发明专利
MACROMONOMER, GRAFT POLYMER AND THEIR PRODUCTION 失效

公开(公告)号：JPH08183760A

公开(公告)日：1996-07-16

申请号：JP32732794

申请日：1994-12-28

申请人： DAIICHI SEIYAKU CO

发明人： AKASHI MITSURU

IPC分类号： C07C235/06 , C07C323/60 , C07C327/20 , C07C327/40 , C08F8/00 , C08F12/00 , C08F212/14 , C08F290/00 , C08F299/00

摘要： PURPOSE: To obtain a macromonomer, having N-isopropylacrylamide in a recurring unit, convertible into a graft copolymer having amphiphilicity and heat- sensitive phase transition properties, etc., and expectable of application to an interfacial modifier, a water-dispersible coating, a drug delivery system, etc. CONSTITUTION: This macromonomer of formula I [Q1 is H or CH3 ; Q2 is a group of formula II or III (R is a 1-10C alkylene); Q3 is 0 or NH; Q4 is R; Q5 is O or S; Y is O or two H atoms; n is 1-50]. The macromonomer of formula I is obtained by radically polymerizing N-isopropylacrylamide in the presence of a chain transfer agent having, e.g. amino, OH or carboxyl in the molecule (e.g. 2-mercaptoethylamine, 2-mercaptoethanol or β-mercaptopropionic acid) and reacting the resultant poly(N-isopropylacrylamide) having terminal amino, OH or carboxyl with a halomethylstyrene or an alkyl methacrylate dioxide.