专利检索_氨基甲酸衍生物即含有如下任何基团的化合物NCOONCO HalNCOONCOHal或NCHalHal或氮原子不属于硝基或亚硝基专利检索_氨基甲酸衍生物即含有如下任何基团的化合物NCOONCO HalNCOONCOHal或NCHalHal或氮原子不属于硝基或亚硝基专利检索查询_氨基甲酸衍生物即含有如下任何基团的化合物NCOONCO HalNCOONCOHal或NCHalHal或氮原子不属于硝基或亚硝基专利检索查询分析平台

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
61	JPS5920642B2 -	JP13745473	1973-12-11	JPS5920642B2	1984-05-15	JON EIPURINGU DAADEN JUNIA; ANTONII ARUMEIDA SUUZA; JON FUAAGASU SUTEIIBUN

62	JPS5822471B2 -	JP12997275	1975-10-30	JPS5822471B2	1983-05-09	MIROSURAFU BUREHA; ZUDENEKU PURICHITA

63	JPS5754503B2 -	JP11685774	1974-10-12	JPS5754503B2	1982-11-18

64	JPS577602B2 -	JP7284074	1974-06-27	JPS577602B2	1982-02-12

65	JPS564543B2 -	JP1291476	1976-02-10	JPS564543B2	1981-01-30

66	Manufacture of llricincarbamate	JP16395479	1979-12-17	JPS5587753A	1980-07-02	JIYAN BURIYU

67	Benzanilides, their preparation and use	JP6783177	1977-06-10	JPS543031A	1979-01-11	SUGANO HIDEO; YABUTANI KUNIHIRO; HARADA TATSUO; HATSUTA SHIGENORI
PURPOSE: Benzanilides I (R ¹ is methyl, trifluoromethyl; R ² is H, isopropoxy; A is H, alkyl, alkanoyl, alkylthiocarbonyl, alkoxycarbonyl, alkyl-substituted carbamoyl). COPYRIGHT: (C)1979,JPO&Japio
68	Phenylamidine derivatives	JP1639078	1978-02-14	JPS53103430A	1978-09-08	LAFON LOUIS

69	Weed killer	JP2939477	1977-03-18	JPS52114020A	1977-09-24	RAINHARUTO HANTE; MANFUREETO KOTSUHO; GERUHARUTO HERURAIN; HERUMUUTO KETSUHIERU; PEETERU RANGERIYUTSUDETSUKE

70	JPS5126432B2 -	JP2877672	1972-03-22	JPS5126432B2	1976-08-06

71	Hannoseihokozokukeiojusurutanryotai oyobi sonojugotainoseizohoho	JP12997275	1975-10-30	JPS5168532A	1976-06-14	MIROSURAFU PUREHA; ZUDENEKU PURICHITA

72	Torikuroruechiriden bisu * isoshianido jikurorido * noseizoho	JP12898075	1975-10-28	JPS5168525A	1976-06-14	GUNTAA BETSUKU

73	JPS5016411B1 -	JP5404269	1969-07-07	JPS5016411B1	1975-06-12

74	JPS4897849A -	JP2877672	1972-03-22	JPS4897849A	1973-12-13

75	JPS4896723A -	JP2998872	1972-03-24	JPS4896723A	1973-12-10

76	바이유레아 제조 공정	KR1020120044892	2012-04-27	KR101420706B1	2014-07-22	허남회; 이병노
본 발명은 고체 히드라진과 유레아를 반응시켜 바이유레아를 제조하는 방법에 관한 것이다. 본 발명에 따른 바이유레아 합성법은 용매 없이 고체 히드라진과 유레아를 고체 상태에서 갈음을 통해서 반응 시키는 것을 특징으로 한다. 본 발명의 바이유레아 합성을 통해 형성되는 부산물인 대표적인 온실 가스인 이산화탄소를 유용한 화합물로 전환하는 기존의 유레아 합성 공정을 더욱 발전시킴으로써 온실가스 배출 저감 효과도 추가로 기대할 수 있다.
77	바이유레아 제조 공정	KR1020120044892	2012-04-27	KR1020130121573A	2013-11-06	허남회; 이병노
The present invention relates to a production method of a biurea compound by making solid hydrazine react with urea. The production method of the biurea compound includes a step of grinding the solid hydrazine and the urea in a solid phase instead of using a solvent for the reaction. By developing a conventional urea synthesis process converting carbon dioxide which is typical greenhouse gas generated from the biurea compound synthesis as a byproduct into useful compounds, a reduction effect for the greenhouse gas can be expected.
78	Electrolyte comprising eutectic mixture with perfluoro ether compound and electrochemical device containing the same	KR20090018619	2009-03-04	KR20100099993A	2010-09-15	HONG YEON SUK; OH JAE SEUNG; LEE BYOUNG BAE; LEE HYO JIN; KIM DONG SU
PURPOSE: An electrolyte containing a fluorinated ether compound, and an electrochemical device including thereof are provided to secure the excellent thermal stability and chemical stability of the electrolyte by including the fluorinated ether compound and an eutectic mixture. CONSTITUTION: An electrolyte contains the following: an eutectic mixture formed with an amide compound marked with either chemical formula 1 or 2, and ionizable lithium salt; and a fluorinated ether compound. In the chemical formula 1, R, R1, and R2 are selected from the group consisting of an alkyl group with 1~20 carbons, hydrogen, halogen, an alkyl amine group, an alkenyl group, and an aryl group.
79	불소화된 카바메이트 및 이소시아네이트의 제조공정	KR1020080090845	2008-09-16	KR1020090028493A	2009-03-18	파디야폴로,아나; 루이즈산타키테리아,발렌틴; 코르마카노스,아벨리노; 가르시아고메즈,헤르메네길도; 후아레즈마린,라켈
A process for producing fluorinated carbamates is provided to obtain fluorinated carbamates with high yield, high purity and high efficiency without using a metallic catalyst, to reduce the catalyst costs and to prevent the environmental contamination. A process for producing fluorinated carbamates comprises the reaction of amine or polyamines and fluoridized carbonates of the chemical formula 1: (OR)(OR')C=O, in the presence of a catalyst having at least one tertiary amine excluding metals. In the chemical formula 1, R and R' are selected from substituted or unsubstituted C1-20 fluorinatd alkyl group.
80	아난드아미드 가수분해 차단을 통한 불안감의 조절	KR1020057005995	2003-10-07	KR1020050088992A	2005-09-07	피오멜리다니엘레; 듀란티안드레아; 톤티니안드레아; 모르마르코; 타르지아조르지오
Fatty acid amide hydrolase inhibitors of the Formula (I) are provided, wherein X is NH, CH2, O, or S; Q is O or S; Z is O or N; R is an aromatic moiety selected from the group consisting of substituted or unsubstituted aryl; substituted or unsubstituted biphenylyl, substituted or unsubstituted naphthyl, and substituted or unsubstituted phenyl; substituted or unsubstituted terphenylyl; substituted or unsubstituted cycloalkyl, heteroaryl, or alkyl; and R1 and R2 are independently selected from the group consisting of H, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, and substituted or unsubstituted phenyl, substituted or unsubstituted biphenylyl, substituted or unsubstituted aryl, and substituted or unsubstituted heteroaryl; with the proviso that if Z is O, one of R1 and R 2 is absent, and that, if Z is N, optionally R1 and R2 may optionally be taken together to form a substituted or unsubstituted N-heterocycle or substituted or unsubstituted heteroaryl with the N atom to which they are each attached. Pharmaceutical compositions comprising the compounds of Formula (I) and methods of using them to inhibit FAAH and/or treat appetite disorders, glaucoma, pain, insomnia, and neurological and psychological disorders including anxiety disorders, epilepsy, and depression are provided.

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