子分类：
| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 1 | FREE RADICAL INHIBITORS FOR QUENCHING AQUEOUS PHASE POLYMER GROWTH AND RELATED METHODS | PCT/US9919355 | 1999-08-24 | WO0011039A2 | 2000-03-02 | |
| An aqueous phase inhibitor for quenching free radical polymerization comprising a free radical quenching agent having a hydrophilic tail is disclosed, as well as a coating and related methods. In one embodiment, the free radical quenching agent can either be an N-hydroxylamine or an N-nitrosonamine, the hydrophilic tail can be a polyhydric alcohol tail and the inhibitor can be a concentrate in a liquid medium such as water, alcohol and mixture thereof. | ||||||
| 2 | 진균 병원체의 방제를 위한 조성물 및 방법 | KR1020117025843 | 2009-04-01 | KR1020120026484A | 2012-03-19 | 피어슨노만; 로스로날드; 어로버트 |
| 식물 병원체 유주자를 유인하는 작용을 할 수 있는 알데히드 및 케톤의 아실히드라존 및 세미카르바존 유도체, 및 이들 화합물의 사용 방법이 본원에 개시된다. 이들 화합물은 화학식 1의 화합물을 포함한다.
<화학식 1> 여기서, X는 (CH 2 ) n , 1,3-페닐렌 및 1,4-페닐렌으로 이루어진 군으로부터 선택되고, R 1 은 이소-부틸, sec-부틸 및 tert-부틸-CH 2 로 이루어진 군으로부터 선택되고, R 2 는 수소 또는 메틸이고, n은 0 내지 25이다. 물에 노출 시, 이들 화합물은 유주자를 유인할 수 있는 알데히드 또는 케톤을 방출한다. 이들 화합물은 난균성 진균 병원체에 대해 특히 효과적인 살진균제 제제를 형성하기 위해 살진균제와 조합될 수 있다. |
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| 3 | 벤조트리아졸의 제조방법 | KR1019840006984 | 1984-11-08 | KR1019910001130B1 | 1991-02-25 | 하가도오루; 나가노에이끼; 다까세마사유끼; 사또료 |
| 내용 없음. | ||||||
| 4 | 2-치환페닐-4, 5, 6, 7-데트라하이드로-2H-인다졸류의 제조방법 | KR1019830004544 | 1983-09-28 | KR1019880000155B1 | 1988-03-12 | 나가노에이끼; 다께모도이찌기; 후꾸시마마사유끼; 요시다료우; 마쯔모도히로시 |
| The title compds. (I) are new. (I) are prepd. by reacting 2, 4- dihalo-5-substd. phenyl-4,5,6,7-tetrahydro-2H-indazole with halo - compds. of formula R-B. In the formula, X=Cl, Br, Y=O or imino gp., Z=Cl or Me, R=C2-4 alkyl, C3-4 alkenyl, C1-6 alkoxycarbonylmethyl, B=halogen. The rxn. is performed at -80 to 200 deg.C for 30mins to 20hdrs in aromatic hydrocarbons (benzene, xylene), halohydrocarbonx(CHCl3, CCl4), ethers(dioxane, THF) in the presence of base i.e. pyridine, NaOH or not. | ||||||
| 5 | N-페닐피라졸 유도체의 제조방법 | KR1019810000606 | 1981-02-24 | KR1019850000993B1 | 1985-07-15 | 에드가윌리암파아넬; 데이빗드앨런로버어츠; 레스리로이헤튼 |
| N-Phenylprazoles of formula I[R5=R6= 1-4C alkyl, trifluoromethyl, nitro, F, Cl or Br; R7 = H, 1-4C alkyl or alkoxy, cyano, F, Cl or Br; R8 = R9 = H, F, Cl. were prepd. by the ring-closing reaction of formula II. The title compds. are preemergent and post emergent herbicides, and they may be used for selective weed control in cereals, soybeans, barley, etc. | ||||||
| 6 | 항우울증 작용을 가진 1,2,4-트리아졸론 화합물 및 그 제조방법 | KR1019840006041 | 1984-09-29 | KR1019850002270A | 1985-05-10 | 리차드이.개맨즈; 데비드더블유.스미드; 조셉피.예비치 |
| 내용없음 | ||||||
| 7 | 치환된 안트라[1,9-Cd]피라졸-6(2H)-온류 및 그 제조방법 | KR1019830003410 | 1983-07-23 | KR1019840005431A | 1984-11-12 | 하워드다니엘홀리스쇼왈터-3 |
| 내용없음 | ||||||
| 8 | 제초제용 N-페닐 피라졸 유도체의 제조 방법 | KR1019830003220 | 1983-07-14 | KR1019840005430A | 1984-11-12 | 레슬리로이하톤-2 |
| 내용없음 | ||||||
| 9 | 치환된 벤즈 아미드의 제조방법 | KR1019850004574 | 1985-06-27 | KR1019920000270B1 | 1992-01-11 | 아이보몬코빅; 데비드윌러 |
| 내용 없음. | ||||||
| 10 | 치환된 안트라[1,9-Cd]피라졸-6(2H)-온류 및 그 제조방법 | KR1019830003410 | 1983-07-23 | KR1019900005026B1 | 1990-07-18 | 하워드다니엘홀리스쇼왈터-3 |
| Substdd anthra (1,9-cd) pyrazol-6(2H)-ones of formyla (I) are prepd. by reacting a cpd of formula (II) with a HNRY. In the formulas, X,X' and W are each H, OH, Cl or C1-4 alkoxy; R is H or C1-6 alkyl; Y is H or substd. OR1 or ANR2R3 C1-6 alkyl; R1 is H or C1-6 alkyl; A is a straight or branched C2-8 alkylene; R2 and R3 are each H, OH substd. alkyl or NRaRa; Ra is H or OH substd. C1-3 alkyl; n and m are each 1-3; Z is H or DNR2R3; D is a OH substd. straight or branched C2-8 alkylene. (I) are useul as antibacterial, antifungal, antitumour and antileukaemia agents. | ||||||
| 11 | 벤조트리아졸의 제조방법 | KR1019840006984 | 1984-11-08 | KR1019850003886A | 1985-06-29 | 하가도오루; 나가노에이끼; 다까세마사유끼; 사또료 |
| 내용없음 | ||||||
| 12 | 치환된 5-아실아미노-1-페닐피라졸의 제조방법 | KR1019840006345 | 1984-10-13 | KR1019850003399A | 1985-06-17 | 라인홀트게링; 에리히클라우케; 오토샬너; 외르크스테터; 한스요아힘잔텔; 로베르트알.슈미트 |
| 내용없음 | ||||||
| 13 | 1,2,4-트리아졸-3-온 항우울증제의 제조방법 | KR840003692 | 1984-06-28 | KR850000430A | 1985-02-27 | |
| 내용없음. | ||||||
| 14 | 금속 레일 블랭크의 성형법 | KR1019840001465 | 1984-03-21 | KR1019840007833A | 1984-12-11 | 쟈끄미쇼 |
| 내용없음. | ||||||
| 15 | N-(1'-하이드로카르보닐옥시카르보닐에틸)-N-알콕시 아세틸 아닐린유도체의 제조방법 | KR1019790003736 | 1979-10-26 | KR1019840000846B1 | 1984-06-19 | 아돌프후벌러; 월터쿤즈; 울프강에카르트 |
| Title compds. I (R1 = C1-4 alkyl, alkoxy, halo; R2 = H, C1-3 alkyl, C1-4 alkoxy, halo; R3 = H, C1-3 alkyl, halo; R4 = H, Me; the sum of C atoms in R1-R4<=6; R5 = C3-6 alkyl or C2-4 alkenyl, C3-4 alkynyl or cycloalkyl; R6 = CH2Z(Z = XR7(X = O, S; R7 = C1-3 alkyl))), useful as agricultural fungicides(no data), were prepd. Thus, 26.5 g N-(1'-carboxyethyl-N-methoxy-acetyl-2,6-dimethyl aniline, 30 g isopropanol and 2g conc. H2SO4 were refluxed for 20 hr and extracted with Me2O to give I (R1, R2 = Me; R3, R4 = H; R5 = Pr; R6 = CH2OCH3). | ||||||
| 16 | N-페닐아민류의 제조방법 | KR1019780000001 | 1978-01-04 | KR1019800001698B1 | 1980-12-31 | 안토니브락숄름클레이톤; 스탄레이카이스레만 |
| Title compds.(I, R = H, halo, nitro, trihalomethyl, C1-7 alkyl, C1-7 alkowy; R1 = H, mono- or di or trihaloacetyl; R2 = C1-7 alkylene, C2-7 alkylidene; Q = carboxy1, C1-7 alkanol ester) were prepd. gy reacting phenylamine(II) and haloalkanoic acid(III) in basic condition followed by reaction of mono- or di- or trihaloacetyl halide(X = halo; n = 0-2 integer to give N-phenylamines. Thus, 2,6-diethylaniline, KOH and DMF were reacted with ethylbromoacetate, extracted washed, dried to give N-(2,6-diethylphenyl)-glycineethyl ester. | ||||||
| 17 | 1-[2-(2,4-디클로로페닐)-펜틸]-1H-1,2,4-트리아졸 및 히드라존 또는 히드라진 유도체의 제조방법 | KR1019830002730 | 1983-06-18 | KR1019910000402B1 | 1991-01-25 | 한스위르크베터-3 |
| 내용 없음. | ||||||
| 18 | 치환된 5-아실아미노-1-페닐피라졸의 제조방법 | KR1019840006345 | 1984-10-13 | KR1019900007179B1 | 1990-09-29 | 라인홀트게링; 에리히클라우케; 오토샬너; 외르크스테터; 한스요아힘잔텔; 로베르트알.슈미트 |
| Herbicidal 5-acylamino-1-phenyl-pyrazole derivs. of the general formula (I) are prepd. by N-acylation of 5-unsubstituted amino-1- phenyl-pyrazoles. In (I), R1 is cyano, alkoxycarbonyl, alkenyloxycarbonyl, alkynyloxycarbonyl, aminocarbonyl, alkylaminocarbonyl, alkenylaminocarbonyl or alkynylaminocarbonyl; R2 is H, alkyl, alkenyl, alkynyl, cycloalkyl, alkoxyalkyl or alkylthioalkyl; R3, R4, R5, R6 and R7 are each H, halogen, cyano, nitro, alkyl, alkylsulfonyl, alkoxycarbonyl or -(X)N-R8; X is O, S, sulfinyl or sulfonyl; n is 0 or 1; R8 is halogenoalkyl. | ||||||
| 19 | 1,2,4-트리아졸-3-온 항우울증제 및 그 제조방법 | KR1019840003692 | 1984-06-28 | KR1019890000637B1 | 1989-03-22 | 데이비스엘.템플,주니어; 윌터지.로베크,주니어 |
| The title cpds. (I)[R=H, halog, alkoxy, CF3; R1=H, alkyl; R2=CH2Ph, (un)substd. Ph, 2-pyridyl, pyrimidyl, 2-quinolinyl, 3benzisothazoyl; x=0, bond; n=2-4 were prepd.. Thus, piperazine (II)(R3=H) was N- alkylated with Br(CH2)3Cl to give 66% (II)[R3= (CH2)3Cl , which was treated with N2H4 to give 92% (II)[R3= (CH2)3NHNH2 . The cyclocondensation of (II) with EtC(S)NHCO2Et gave 72% piperazinopropyltriazole (III)(R4=H), which was Nalkylated with PhOCH2CH2Br to give 53% (III)(R4=CH2CH2OPh)(IV). (IV) is an antidepressant with minimal potential for side effects such as sedation and blood pressure lowering. | ||||||
| 20 | 항우울증 작용을 가진 1,2,4-트리아졸론 화합물 및 그 제조방법 | KR1019840006041 | 1984-09-29 | KR1019880002624B1 | 1988-12-07 | 리차드이.개맨즈; 데비드더블유.스미드; 조셉피.예비치 |
| 2-[3-[4-(3-halophenyl)-1-piperatinyl propyl -5-(1hydroxyethyl)-2,4- dihydro-4-phenoxyalkyl-3H-1,2,4-triazol-3-ones of formula (I) or their pharmaceutically acceptable salts are prepd.. In the formula (I), Y is halogen or CF3; Z is H or (II) [R'=H, halogen, lower alkoxy or CF3 ; n is 2-4. (I) are useful as selective antidepressants. | ||||||
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