相似化合物
95034-05-2 320581-09-7 15444-85-6欧盟法规
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2,2-dimethylaziridine α-amino-isobutyraldehyde-oxime 2-nitro-2-methylpropanol N,N'-(1,1-dimethyl-ethanediyl)-bis-acetamideN,N'-(1,1-dimethyl-ethanediyl)-bis-acetamide 2-methyl-1,2-bis-(3-nitro-benzoylamino)-propane decane8-benzoyl-2,2-dimethyl-1,4,8-triazaspiro4.5decane 2-Methyl-1,2-bis(tosylamino)propan 1,1-Dimethyl-2-(amin°Carbonylamino)ethylamine 合成工艺路线路线简述
- 69894-12-8 = 811-93-8
反应条件:1.1 Reagents: Potassium Hydroxide Solvents: Water; 12 H,Rt -> 104 °C1.2 Reagents: Potassium Hydroxide; 3 H,35 °C1.3 Reagents: Sodium; 2 H,65 °C
标题:Synthesis Of 2-Methyl-1,2-Diaminopropane
作者:Lu,Fei; Et Al
参考文献:Huaxue Shijie 日期:2011 卷标:52(12) 页码:728-730]
24884-68-2 = 811-93-8
反应条件:1.1 Reagents: Hydrogen Catalysts: Platinum Solvents: Acetic Acid
标题:Addition Of Dinitrogen Tetroxide To Olefins. Iv. Butylenes
作者:Levy,Norman; Et Al
参考文献:Journal Of The Chemical Society 日期:1948 卷标:52 页码:52-60]
90304-06-6 = 811-93-8 [标题:Reaction Conditions
标题:Product Subclass 4: N-Nitrogen- Or N-Phosphorus-Functionalized Alkylamines (N >=2)
作者:Roy,K.-M.
参考文献:Science Of Synthesis 日期:2009 卷标:40 页码:615-641]
40652-06-0 = 811-93-8
反应条件:1.1 Reagents: Hydrogen Catalysts: Nickel Solvents: Methanol1.2 Reagents: Sodium Hydroxide Solvents: Water
标题:Preparation Of 2-Methyl-1,3-Propanediamine
参考文献:Japan]
40652-06-0 = 811-93-8
反应条件:1.1 Reagents: Hydrogen,Ammonium Hydroxide Catalysts: Nickel Solvents: Methanol; Rt -> 90 °C; 10 H,0.9 - 1.0 Mpa,85 - 90 °C2.1 Reagents: Potassium Hydroxide Solvents: Water; 12 H,Rt -> 104 °C2.2 Reagents: Potassium Hydroxide; 3 H,35 °C2.3 Reagents: Sodium; 2 H,65 °C
标题:Synthesis Of 2-Methyl-1,2-Diaminopropane
作者:Lu,Fei; Et Al
参考文献:Huaxue Shijie 日期:2011 卷标:52(12) 页码:728-730]
2305-59-1 = 811-93-8 [标题:Reaction Conditions
标题:Product Subclass 4: N-Nitrogen- Or N-Phosphorus-Functionalized Alkylamines (N >=2)
作者:Roy,K.-M.
参考文献:Science Of Synthesis 日期:2009 卷标:40 页码:615-641]
95647-95-3 = 811-93-8 [标题:Reaction Conditions
标题:Product Subclass 4: N-Nitrogen- Or N-Phosphorus-Functionalized Alkylamines (N >=2)
作者:Roy,K.-M.
参考文献:Science Of Synthesis 日期:2009 卷标:40 页码:615-641]
90304-06-6 = 811-93-8 [标题:Reaction Conditions
标题:Product Subclass 4: N-Nitrogen- Or N-Phosphorus-Functionalized Alkylamines (N >=2)
作者:Roy,K.-M.
参考文献:Science Of Synthesis 日期:2009 卷标:40 页码:615-641]
19355-69-2 = 811-93-8
反应条件:1.1 0 - 5 °C; 2 H,5 °C -> 40 °C1.2 Catalysts: 4-(Dimethylamino)Pyridine; 2 H,40 °C2.1 Reagents: Hydrogen,Ammonium Hydroxide Catalysts: Nickel Solvents: Methanol; Rt -> 90 °C; 10 H,0.9 - 1.0 Mpa,85 - 90 °C3.1 Reagents: Potassium Hydroxide Solvents: Water; 12 H,Rt -> 104 °C3.2 Reagents: Potassium Hydroxide; 3 H,35 °C3.3 Reagents: Sodium; 2 H,65 °C
标题:Synthesis Of 2-Methyl-1,2-Diaminopropane
作者:Lu,Fei; Et Al
参考文献:Huaxue Shijie 日期:2011 卷标:52(12) 页码:728-730]
420-04-2 = 811-93-8 [标题:Reaction Conditions
标题:Product Subclass 4: N-Nitrogen- Or N-Phosphorus-Functionalized Alkylamines (N >=2)
作者:Roy,K.-M.
参考文献:Science Of Synthesis 日期:2009 卷标:40 页码:615-641
N-氰基-N'-甲基乙脒置于lithium Aluminium Tetrahydride体系中,用 乙醚 作为反应溶剂,化学反应 5.0H,反应生成 1,2-二氨基-2-甲基丙烷
参考文献:具有构型手性的混合二胺钯(II)配合物的光学分辨率和圆二色光谱
标题:具有构型手性的混合二胺钯(II)配合物的光学分辨率和圆二色光谱
摘要:六个方形平面配合物,[pdl(Meso-Stien)](Clo4)2(meso-Stien=meso-1,2-Diphenyl-1,2-乙二胺;l=n,N-二乙基乙二胺,N,N-二甲基乙二胺,2-甲基-1,2-丙二胺,N2,N2-二甲基-2-甲基-1,2-丙二胺,N,N-二甲基-1,3-丙二胺,和 (2S)-N1,N1Diethyl-1,2-丙二胺),使用二乙酰-D-酒石酸酐作为拆分剂进行光学拆分(或在最后命名的配体的情况下分离).测量了它们的电子吸收和 Cd 光谱.由于 (2S)-N1,N1-二乙基-1,2-丙二胺络合物中的不对称碳原子,手性构型引起的构型 Cd 和邻位 Cd 之间已证实明确的可加性.
DOI:10.1246/bcsj.54.1056
专利信息
专利号:WO-9837078-A1
优先权日:1997-02-20
标题 :Solid phase and combinatorial synthesis of substituted thiophenes and of arrays of substituted thiophenes
发明人:DOERWALD FLORENCIO ZARAGOZA
权利人:NOVO NORDISK AS
摘要:A solid phase method for the synthesis of a plurality of differently substituted thiophenes with a wide variety of side-chain substituents as compounds of potential therapeutic interest. The thiophenes are prepared by reaction of a substrate-bound primary or secondary amine with a thiophosgene equivalent and reaction of the resulting intermediate with an acceptor-substituted acetonitrile in the presence of a base. Alkylation with an appropriate alkyl halide, followed by Thorpe-Ziegler-cyclization yields differently substituted, support-bound 3-aminothiophenes. These may be screened on the substrate or cleaved from the substrate and then screened in solution. Alternatively, the resin-bound 3-amino thiophenes or the synthetic intermediates can be subjected to further synthetic transformations (N-acylation, reduction) on the support, which permits the preparation of further therapeutically interesting compounds. The efficient synthesis of a wide variety of thiophenes using automated synthesis technology of the present method makes these compounds attractive candidates for the generation and rapid screening of diverse thiophene-based libraries. The method disclosed here provides an easy and fast access to highly diverse heterocyclic compounds of therapeutic interest, amenable to automatization.
专利号:US-5877278-A
优先权日:1992-09-24
标题:Synthesis of N-substituted oligomers
发明人:ZUCKERMANN RONALD N; GOFF DANE A; NG SIMON; SPEAR KERRY; SCOTT BARBARA O; SIGMUND AARON C; GOLDSMITH RICHARD A; MARLOWE CHARLES K; PEI YAZHONG; RICHTER LUTZ; SIMON REYNA
权利人:CHIRON CORP
摘要:A solid-phase method for the synthesis of N-substituted oligomers, such as poly (N-substituted glycines) (referred to herein as poly NSGs) is used to obtain oligomers, such as poly NSGs of potential therapeutic interest which poly NSGs can have a wide variety of side-chain substituents. Each N-substituted glycine monomer is assembled from two 'sub-monomers' directly on the solid support. Each cycle of monomer addition consists of two steps: (1) acylation of a secondary amine bound to the support with an acylating agent comprising a leaving group capable of nucleophilic displacement by -NH2, such as a haloacetic acid, and (2) introduction of the side-chain by nucleophilic displacement of the leaving group, such as halogen (as a solid support-bound alpha -haloacetamide) with a sufficient amount of a second sub-monomer comprising an -NH2 group, such as a primary amine, alkoxyamine, semicarbazide, acyl hydrazide, carbazate or the like. Repetition of the two step cycle of acylation and displacement gives the desired oligomers. The efficient synthesis of a wide variety of oligomeric NSGs using automated synthesis technology of the present method makes these oligomers attractive candidates for the generation and rapid screening of diverse peptidomimetic libraries. The oligomers of the invention, such as N-substituted glycines (i.e. poly NSGs) disclosed here provide a new class of peptide-like compounds not found in nature, but which are synthetically accessible and have been shown to possess significant biological activity and proteolytic stability. Combinatorial libraries of cyclic compounds are disclosed wherein the cyclic compounds are comprised of at least one ring structure derived from cyclization of a peptoid backbone. The diversity of product compounds is generated by the sequential addition of substituted submonomers. The combinatorial library includes 10 or more, preferably 100 or more, and more preferably 1,000 or more distinct and different compounds. The library includes each of the product compounds in retrievable and analyzable amounts and preferably includes at least one biologically active compound. Methods of synthesizing the combinatorial libraries and assay devices produced using the libraries are disclosed as is methodology for screening for and obtaining biologically active cyclic organic compounds.
专利号:WO-2025134140-A1
优先权日:2023-12-19
标题:A method for the synthesis of substituted anthranilic amide compounds, intermediates and salts thereof
发明人:MALVIYA NITIN JAIKANT; SINGH VIPENDER; SHAH JIGARKUMAR HARKISHANDAS; KALE MANOJ GANPAT; KAVITAKE SANTOSH GIRIDHAR; BORHADE AJIT SAHEBRAO; KLAUSENER ALEXANDER G M
权利人:PI INDUSTRIES LTD
摘要:The present invention discloses a method for the synthesis of compounds of formula (I) or a salt thereof, wherein, R is selected from hydrogen, halogen, cyano, C1-C12 alkyl, C1-C12 haloalkyl, C1-C12 alkoxy, C1-C12 haloalkoxy, or C3-C8 cycloalkyl; R4 is selected from hydrogen, C1-C12 alkyl, C2-C12 alkenyl, C2-C12 alkynyl, C1-C12 haloalkyl, C2-C12 haloalkenyl, C2-C12 haloalkynyl, C1-C12 alkoxy, C1-C12 haloalkoxy, C3-C8 cycloalkyl, or C3-C8 cycloalkyl-C1-C10 alkyl; and n represents an integer selected from 0-4. The method further comprises the synthesis of an anthranilic diamide compound of formula (A).
专利号:WO-2025134143-A1
优先权日:2023-12-19
标题 :A method for the synthesis of substituted anthranilic amide compounds, intermediates and salts thereof
发明人:MALVIYA NITIN JAIKANT; SINGH VIPENDER; MAL SANJIB; YADAV SANTOSH; SHAH JIGARKUMAR HARKISHANDAS; KAVITAKE SANTOSH GIRIDHAR; BORHADE AJIT SAHEBRAO; KLAUSENER ALEXANDER G M
权利人:PI INDUSTRIES LTD
摘要:The present invention discloses a method for the synthesis of compounds of formula (I) or a salt thereof, wherein R is selected from hydrogen, halogen, cyano, C1-C12 alkyl, C1-C12 haloalkyl, C1-C12 alkoxy, C1-C12 haloalkoxy, or C3-C8 cycloalkyl; R4 is selected from hydrogen, C1-C12 alkyl, C2-C12 alkenyl, C2-C12 alkynyl, C1-C12 haloalkyl, C2- C12 haloalkenyl, C2-C12 haloalkynyl, C1-C12 alkoxy, C1-C12 haloalkoxy, C3-C8 cycloalkyl, or C3-C8 cycloalkyl-C1-C10 alkyl; and n represents an integer selected from 0-4. The process further comprises the synthesis of an anthranilic diamide compound of formula (A).
专利号:WO-2015193910-A1
优先权日:2014-06-20
标题:Asymmetric synthesis of 2-substituted indolines and 3-substituted cinnolines
发明人:KUMAR BOOPATHY SENTHIL; SUDALAI ARUMUGAM
权利人:COUNCIL SCIENT IND RES
摘要:The present invention relates to a novel one step proline catalyzed process for synthesis of chiral hydrazine and its derivatives from o-bromo hydro cinamaldehyde. Further, it relates to a novel one step process for the synthesis of substitued indolines and cinnolines from chiral hydrazines and its derivatives.
专利号:WO-2016173960-A1
优先权日:2015-04-29
标 题 :Optimized synthesis of pregabalin and 4-aminobutane acid using an improved method for producing conjugated nitroalkenes
发明人:STUMPF MARCUS
权利人:K H S PHARMA HOLDING GMBH
摘要:The invention relates to an optimized synthesis of pregabalin and additional 4-aminobutane acids using an improved method for producing conjugated nitroalkenes. This is achieved by a nitro-aldol reaction of an aliphatic aldehyde with a nitroalkane in the presence of a suitable diamine directly followed by an elimination of the conjugated nitroalkene by adding an acid, a subsequent catalyzed asymmetrical 1,4-Michael addition of a suitable nucleophile, and a subsequent retro-Claisen reaction or a hydrolosis and decarboxylation with a concluding reduction to 4-aminobutane acid.