- 英文名称Cis-Cyclohexane-1,2-Diamine
- 中文名称顺式-1,2-环己二胺
- IUPAC名称(1R,2S)-cyclohexane-1,2-diamine
- 其它别名Cis-1,2-Cyclohexanediamine; R0Zn6K26Ep; (R)(S)-1,2-Diaminocyclohexane; 1,2-Cyclohexanediamine,(1R,2S)-Rel-; Cis-Cyclohexane-1,2-Diamine; 1,2-Cis-Diamino-Cyclohexane; 1,2-Cyclohexanediamine, Cis-; Inchi=1/c6H14N2/
- CAS编号1436-59-5
- MFCD编号:MFCD00063746
- EINECS号:604-372-0
- FDA UNII编号:R0ZN6K26EP
- 分子式:C6H14N2
- 分子量:114.19
- 产品CID: 665246
- 产品分类化学试剂 → 有机试剂 → 酰亚胺
欧盟法规
REACH注册ECHA物质C&L通报REACH预注册上下游产品
CAS号317595-54-3 (2-氨基环己基)氨基甲酸叔丁酯 | CAS号36818-07-2 3-氧代-3,4-二氢-2-喹... | CAS号365996-30-1 (1S,2R)-N1-(叔丁氧... | CAS号2562-37-0 1-硝基环己烯 | CAS号184954-75-4 顺-N1-叔丁氧羰基-1,2-环己二胺 | CAS号90605-88-2 1,2-Cyclohexane...专利信息
专利号:US-8735586-B2
优先权日:2007-06-26
标 题 :Regioselective copper catalyzed synthesis of benzimidazoles and azabenzimidazoles
发明人:ALONSO JORGE; LINDENSCHMIDT ANDREAS; NAZARÉ MARC; URMANN MATTHIAS; HALLAND NIS; RKYEK OMAR
权利人:ALONSO JORGE; LINDENSCHMIDT ANDREAS; NAZARÉ MARC; URMANN MATTHIAS; HALLAND NIS; RKYEK OMAR; SANOFI SA
摘要:The present invention relates to a process for the regioselective synthesis of compounds of the formula I, n nwherein R0; R1; R2; R3; R4; R5; A1; A2; A3; A4, Q and J have the meanings indicated in the claims. The present invention provides a direct copper catalyzed regioselective process to a wide variety of unsymmetrical, multifunctional N-substituted benzimidazoles or azabenzimidazoles of formula I starting from 2-halo-nitroarenes and N-substituted amides.
专利号:EP-2173747-B1
优先权日:2007-06-26
标 题:A regioselective metal catalyzed synthesis of annelated benzimidazoles and azabenzimidazoles
发明人:ALONSO JORGE; LINDENSCHMIDT ANDREAS; NAZARE MARC; R KYEN OMAR; URMANN MATHIAS; HALLAND NIS
权利人:SANOFI SA
摘要:The present invention relates to a process for the regioselective synthesis of compounds of the formula I, wherein R1; R2; R3; R4; J1; J2; J3; J4 and G have the meanings indicated in the claims. The present invention provides a direct metal, e.g. palladium or copper, catalyzed, regioselective process to a wide variety of unsymmetrical, multifunctional N-substituted benzimidazoles or azabenzimidazoles of formula I starting from 2-halo-nitroarenes and N-substituted amides.
专利号:US-4711957-A
优先权日:1979-07-13
标题 :Synthesis of 2-keto-1,4-diazacycloalkanes
发明人:LAI JOHN T
权利人:GOODRICH CO B F
摘要:The disclosure deals with novel synthesis involving (a) hydrogenation of a cis-3,3-dialkyl-3,4-dihydroquinoxaline-2-one in the presence of a suitable hydrogenation catalyst, at elevated temperature and pressure, to yield a cis-3,3-dialkyl decahydroquinoxaline-2-one; (b) reaction of trans-1,2-diaminocyclohexane with acetone cyanohydrin in the presence of water to yield trans-3,3-dimethyl-decahydroquinoxaline-2-one; and (c) a reaction of 1,2-diamine with a saturated acyclic or cyclic monoketone or aldehyde and a holoform, in the presence of (i) a phase transfer catalyst (ii) an organic solvent, and (iii) solid or aqueous alkali to yield 2-keto-1,4-diazacycloalkanes. Such compounds exhibit exceptional UV light stabilizing property.
专利号:US-6413957-B1
优先权日:1998-04-21
标题:Methods of inhibiting cell proliferation using indeno [1,2-c]pyrazol-4-ones
发明人:NUGIEL DAVID A; CARINI DAVID J; DI MEO SUSAN V; YUE EDDY W
权利人:BRISTOL MYERS SUIBB PHARMA COM
摘要:The present invention relates to the synthesis of a new class of indeno[1,2-c]pyrazol-4-ones of formula (I): n that are potent inhibitors of the class of enzymes known as cyclin dependent kinases, which relate to the catalytic subunits cdk1-7 and their regulatory subunits know as cyclins A-G. This invention also provides a novel method of treating cancer or other proliferative diseases by administering a therapeutically effective amount of one of these compounds or a pharmaceutically acceptable salt form thereof. Alternatively, one can treat cancer or other proliferative diseases by administering a therapeutically effective combination of one of the compounds of the present invention and one or more other known anti-cancer or anti-proliferative agents.
专利号:US-4806648-A
优先权日:1986-12-18
标题 :Efficient synthesis of cyclic cis-vicinal teritiary diamines
发明人:ROSENZWEIG HOWARD; FRAENKEL GIDEON
权利人:UNIV OHIO STATE RES FOUND
摘要:The one aspect of this invention relates to a process for making cis-vicinal tertiary diamines of general formula: ##STR1## wherein n is from 2-8, and NR 21 is selected from a group including N-piperidino, N-pyrrolidino, dialkylamino containing C 1 -C 12 straight or branched alkyl groups optionally substituted by C 3 -C 7 cycloalkyl groups. The process comprises the formation of a cyclic aminoenamine and the stereospecific catalytic hydrogenation of cyclic aminoenamine to a cis diamine. Another aspect of this invention involves the uses of cis-vicinal tertiary diamines as catalysts of organolithium initiated anionic polymerization of 1,3-dienes, as anti-neoplastic agents and as bacteriacides.
专利号:US-2006025421-A1
优先权日:2004-06-25
标 题:Pyridyl piperazines for the treatment of CNS disorders
发明人:BRODNEY MICHAEL A
权利人:PFIZER
摘要:This invention is directed to compounds of Formula I and to pharmaceutical compositions comprising the compound of Formula I. n n where the dashed line represents an optional double bond; and where n is 1 or 2, and Ar 1 , Ar 2 , . . . and Z are as defined in the specification. The invention is also directed to a method of treating a disorder or condition that can be treated by altering serotonin-mediated neurotransmission, such as migraine, headache, cluster headache, anxiety, depression, etc. This invention is also directed to intermediates useful in the synthesis of compounds of Formula I.