1603-40-3 + 1878-67-7 = 1603-40-3 + 81316-36-1 反应条件:1.1 Reagents: 1-Hydroxybenzotriazole,1-Ethyl-3-(3′-Dimethylaminopropyl)Carbodiimide Hydrochloride Solvents: Tetrahydrofuran; Overnight,25 °C2.1 Reagents: Oxygen Catalysts: Cupric Acetate Solvents: 1,2-Dichloroethane; 6 H,80 °C 标题:Copper-Catalyzed Transamidation Of Unactivated Secondary Amides Via C-H And C-N Bond Simultaneous Activations 作者:Lv,Cong; Et Al 参考文献:Journal Of Organic Chemistry 日期:2023 卷标:88(4) 页码:2140-2157]
= 1603-40-3 + 81316-36-1 反应条件:1.1 Reagents: Oxygen Catalysts: Cupric Acetate Solvents: 1,2-Dichloroethane; 6 H,80 °C2.1 Reagents: 1-Hydroxybenzotriazole,1-Ethyl-3-(3′-Dimethylaminopropyl)Carbodiimide Hydrochloride Solvents: Tetrahydrofuran; Overnight,25 °C3.1 Reagents: Oxygen Catalysts: Cupric Acetate Solvents: 1,2-Dichloroethane; 6 H,80 °C 标题:Copper-Catalyzed Transamidation Of Unactivated Secondary Amides Via C-H And C-N Bond Simultaneous Activations 作者:Lv,Cong; Et Al 参考文献:Journal Of Organic Chemistry 日期:2023 卷标:88(4) 页码:2140-2157]
2761761-94-6 = 1603-40-3 + 84194-36-5 反应条件:1.1 Catalysts: Cupric Acetate Solvents: 1,2-Dichloroethane; 6 H,Rt 标题:From Amides To Urea Derivatives Or Carbamates With Chemospecific C-C Bond Cleavage At Room Temperature 作者:Lv,Cong; Liu,Dan; Muschin,Tegshi; Bai,Chaolumen; Bao,Agula; Et Al 参考文献:Organic Chemistry Frontiers 日期:2022 卷标:9(5) 页码:1354-1363]
= 1603-40-3 + 81316-36-1 反应条件:1.1 Reagents: Oxygen Catalysts: Cupric Acetate Solvents: 1,2-Dichloroethane; 6 H,80 °C 标题:Copper-Catalyzed Transamidation Of Unactivated Secondary Amides Via C-H And C-N Bond Simultaneous Activations 作者:Lv,Cong; Et Al 参考文献:Journal Of Organic Chemistry 日期:2023 卷标:88(4) 页码:2140-2157]
1003-03-8 = 1603-40-3 + 81316-36-1 反应条件:1.1 Reagents: Oxygen,Tetrabutylammonium Hydrogen Sulfate Catalysts: Cupric Acetate Solvents: Acetonitrile; 6 H,80 °C2.1 Reagents: 1-Hydroxybenzotriazole,1-Ethyl-3-(3′-Dimethylaminopropyl)Carbodiimide Hydrochloride Solvents: Tetrahydrofuran; Overnight,25 °C3.1 Reagents: Oxygen Catalysts: Cupric Acetate Solvents: 1,2-Dichloroethane; 6 H,80 °C 标题:Copper-Catalyzed Transamidation Of Unactivated Secondary Amides Via C-H And C-N Bond Simultaneous Activations 作者:Lv,Cong; Et Al 参考文献:Journal Of Organic Chemistry 日期:2023 卷标:88(4) 页码:2140-2157]
= 1603-40-3 + 81316-36-1 反应条件:1.1 Reagents: Oxygen,Tetrabutylammonium Hydrogen Sulfate Catalysts: Cupric Acetate Solvents: Acetonitrile; 6 H,80 °C2.1 Reagents: 1-Hydroxybenzotriazole,1-Ethyl-3-(3′-Dimethylaminopropyl)Carbodiimide Hydrochloride Solvents: Tetrahydrofuran; Overnight,25 °C3.1 Reagents: Oxygen Catalysts: Cupric Acetate Solvents: 1,2-Dichloroethane; 6 H,80 °C 标题:Copper-Catalyzed Transamidation Of Unactivated Secondary Amides Via C-H And C-N Bond Simultaneous Activations 作者:Lv,Cong; Et Al 参考文献:Journal Of Organic Chemistry 日期:2023 卷标:88(4) 页码:2140-2157]
100-51-6 = 1603-40-3 + 81316-36-1 反应条件:1.1 Reagents: Oxygen Catalysts: Cupric Acetate Solvents: 1,2-Dichloroethane; 6 H,80 °C2.1 Reagents: 1-Hydroxybenzotriazole,1-Ethyl-3-(3′-Dimethylaminopropyl)Carbodiimide Hydrochloride Solvents: Tetrahydrofuran; Overnight,25 °C3.1 Reagents: Oxygen Catalysts: Cupric Acetate Solvents: 1,2-Dichloroethane; 6 H,80 °C 标题:Copper-Catalyzed Transamidation Of Unactivated Secondary Amides Via C-H And C-N Bond Simultaneous Activations 作者:Lv,Cong; Et Al 参考文献:Journal Of Organic Chemistry 日期:2023 卷标:88(4) 页码:2140-2157]
= 1603-40-3 + 81316-36-1 反应条件:1.1 Reagents: Oxygen,Tetrabutylammonium Hydrogen Sulfate Catalysts: Cupric Acetate Solvents: Acetonitrile; 6 H,80 °C2.1 Reagents: 1-Hydroxybenzotriazole,1-Ethyl-3-(3′-Dimethylaminopropyl)Carbodiimide Hydrochloride Solvents: Tetrahydrofuran; Overnight,25 °C3.1 Reagents: Oxygen Catalysts: Cupric Acetate Solvents: 1,2-Dichloroethane; 6 H,80 °C 标题:Copper-Catalyzed Transamidation Of Unactivated Secondary Amides Via C-H And C-N Bond Simultaneous Activations 作者:Lv,Cong; Et Al 参考文献:Journal Of Organic Chemistry 日期:2023 卷标:88(4) 页码:2140-2157]
1017324-23-0 = 1603-40-3 + 81316-36-1 反应条件:1.1 Reagents: Oxygen,Tetrabutylammonium Hydrogen Sulfate Catalysts: Cupric Acetate Solvents: Acetonitrile; 6 H,80 °C2.1 Reagents: 1-Hydroxybenzotriazole,1-Ethyl-3-(3′-Dimethylaminopropyl)Carbodiimide Hydrochloride Solvents: Tetrahydrofuran; Overnight,25 °C3.1 Reagents: Oxygen Catalysts: Cupric Acetate Solvents: 1,2-Dichloroethane; 6 H,80 °C 标题:Copper-Catalyzed Transamidation Of Unactivated Secondary Amides Via C-H And C-N Bond Simultaneous Activations 作者:Lv,Cong; Et Al 参考文献:Journal Of Organic Chemistry 日期:2023 卷标:88(4) 页码:2140-2157
专利号:US-7179919-B2 优先权日:2004-03-18 标 题 :Stereoselective synthesis of certain trifluoromethyl-substituted alcohols 发明人:SONG JINHUA J; TAN ZHULIN; YEE NATHAN K; SENANAYAKE CHRIS HUGH; XU JINGHUA; GALLOU FABRICE 权利人:BOEHRINGER INGELHEIM PHARMA 摘要:A process for stereoselective synthesis of a compound of Formula (I) n nwherein R 1 , R 2 , R 3 , R 4 , and R 5 are as described herein.
专利号:US-7425629-B2 优先权日:2005-09-30 标 题:Stereoselective synthesis of certain trifluoromethyl-substituted alcohols 发明人:SONG JINHUA J; REEVES JONATHAN T; ROSCHANGAR FRANK; TAN ZHULIN; YEE NATHAN K 权利人:BOEHRINGER INGELHEIM PHARMA 摘要:A process for stereoselective synthesis of a compound of Formula (I) n nwherein R 1 , R 2 , R 3 , R 4 , and R 5 are as described herein.
专利号:US-2011224405-A1 优先权日:2008-11-14 标 题:Degradable supports for tide synthesis 发明人:LIVINGSTON ANDREW GUY; PEEVA LUDMILA GEORGIEVA; SO SHEUNG 权利人:IMP INNOVATIONS LTD 摘要:According to the present invention, there is provided a process for synthesis of a first compound selected from peptides, oligonucleotides, and peptide nucleic acids, which comprises synthesis of the first compound linked to a soluble support, wherein the soluble support is degraded following the synthesis so that it can be separated from the first compound.
专利号:US-7371769-B2 优先权日:2004-12-07 标 题 :Tetrahydropyridin-4-yl indoles with a combination of affinity for dopamine-D2 receptors and serotonin reuptake sites 发明人:HES ROELOF VAN; SMID PIETER; KRUSE CORNELIS G; TULP MARTINUS TH M 权利人:SOLVAY PHARM BV 摘要:The present invention relates to a group of novel tetrahydropyridin-4-yl indoles with a dual mode of action: serotonin reuptake inhibition and affinity for dopamine-D 2 receptors, to methods for the preparation of these compounds and to novel intermediates useful for the synthesis of said tetrahydropyridin-4-yl indoles. The invention also relates to the use of a compound disclosed herein for the manufacture of a medicament giving a beneficial effect. n The invention relates to novel tetrahydropyridin-4-yl indoles of the formula. n nand tautomers, stereoisomers, prodrugs, N-oxides, pharmacologically acceptable salts, hydrates and solvates thereof,n nwherein:n R 1 is hydrogen, halogen, alkyl(C 1-3 ) or alkoxy(C 1-3 ), CN or CF 3 , R 2 is hydrogen or alkyl(C 1-3 ), R 3 is hydrogen or alkyl(C 1-3 ), Z is hydrogen or alkyl(C 1-3 ), alkoxy(C 1-3 ) or alkylthio(C 1-3 ), A is hydrogen or alkyl(C 1-3 ), or A and Z together form a saturated or (partly) unsaturated 5- or 6-membered ring which may be substituted with halogen, alkyl (C 1-3 ) or phenyl, in which ring Z represents carbon, sulfur of nitrogen.
专利号:US-5681959-A 优先权日:1995-02-21 标题:Chemical synthesis of azaindoles 发明人:BISHOP BRIAN CCHRISTOPHER; COTTRELL IAN FRANK; CAMERON MARK; HANDS DAVID 权利人:MERCK SHARP & DOHME 摘要:The present invention relates to a process for the preparation of azaindole derivatives of the formula ##STR1## wherein Q is hydrogen, C 1-6 alkyl, C 2-6 alkenyl, C 1-6 alkoxy, hydroxy, aryl or arylC 1-4 alkyl; n one of X, Y and Z is --Nâ• and the others are --CHâ• ; n R 1 is hydrogen, C 1-6 alkyl, C 2-6 alkenyl or C 1-6 alkyl substituted by a group selected from aryl or --NR 2 R 3 where R 2 and R 3 each independently represent C 1-4 alkyl, or R 2 and R 3 , together with the nitrogen atom to which they are attached, form a 4-7 membered saturated heterocyclic ring, optionally containing in the ring an oxygen or sulphur atom or a group NR 4 where R 4 is C 1-4 alkyl, aryl or arylC 1-4 alkyl; and n R 5 is a hydrogen atom or a group selected from C 1-6 alkyl or aryl.
专利号:US-4963681-A 优先权日:1987-07-06 标题:Process for synthesis of aminomethylene phosphonoalkylphosphinates 发明人:EBETINO FRANK H 权利人:NORWICH EATON PHARMA 摘要:The present invention involves processes for making aminomethylene phosphonoalkylphosphinate compounds comprising: n (a) heating a substantially anhydrous mixture comprising an amine, an ester of an alkyl phosphite, and an ester of a phosphate acetal; and then n (b) adding water to the mixture.
[参考文献]: Cengiz Yenikaya, Et Al. Synthesis And Characterisation Of Two Novel Proton Transfer Compounds And Their Inhibition Studies On Carbonic Anhydrase Isoenzymes. J Enzyme Inhib Med Chem. 2011 Feb;26(1):104-14. [参考文献]: T G Altuntas, Et Al. Comutagenesis-I: The In Vitro Metabolism Of 2-Amino-3-Methylpyridine. Anticancer Res. 1997 Sep-Oct;17(5A):3485-91. [参考文献]: T G Altuntas, Et Al. Comutagenesis-Iii. In Vitro Metabolism Of 2-Amino-3-Methylpyridine: The Effect Of Various Potential Inhibitors, Activators And Inducers. Xenobiotica. 1997 Nov;27(11):1103-11. [参考文献]: T G Altuntas, Et Al. Comutagenesis-Iv In Vitro Metabolism Of The Comutagen 2-Amino-3-Methylpyridine: Species Differences And Metabolic Interaction With Norharman. Anticancer Res. 1997 Nov-Dec;17(6D):4479-82.
合成参考文献
参考文献:10.1107/s1600536811012116 摘要:Yuan XL. 2-Eth-oxy-6-[(3-methyl-pyridin-2-yl)-imino-meth-yl]phenol. Acta Crystallogr Sect E Struct Rep Online. 2011 May 01;67(Pt 5):o1064.