专利号:US-6750335-B2 优先权日:1999-10-29 标 题 :Nucleoside derivatives with photolabile protective groups 发明人:PFLEIDERER WOLFGANG; BUEHLER SIGRID; GIEGRICH HEINER 权利人:NIGU CHEMIE GMBH 摘要:The invention relates to nucleoside derivatives with photolabile protecting groups of general formula (I) n wherein n R 1 is H, F, Cl, Br, I, or NO 2 ; R 2 is H or CN, provided that R 1 and R 2 are not simultaneously H; R 3 is H, 1-4 C alkyl, or phenyl; R 4 is H or a conventional functional group for the synthesis of oligonuleotides; R 5 is H, OH, halogen or XR 6 , where X=O or S, and R 6 is a conventional nucleotide protecting group; and B is adenine, cytosine, guanine, thymine, uracil, 2,6-diaminopurin-9-yl, hypoxanthin-9-yl, 5-methylcytosin-1-yl, 5-amino-4-imidazolcarboxamid-1-yl or 5-amino-4-imidazolcarboxamid-3-yl, where, if B is adenine, cytosine or guanine the primary amine functionality, optionally, carries a permanent protecting group. Furthermore, these derivatives may be used for the light-controlled synthesis of oligonucleotides on a DNA chip.
专利号:US-6153744-A 优先权日:1996-05-20 标 题 :Nucleoside derivatives with photolabile protective groups 发明人:PFLEIDERER WOLFGANG; BUEHLER SIGRID 权利人:WOLFGANG PFLEIDERER 摘要:The invention relates to nucleo-side derivatives with photo-unstable protective groups of the general formula (I) in which R1 is H, NO2, CN, OCH3, halogen, alkyl or alkoxyalkyl with 1 to 4 C atoms, R2 is H, OCH3, R3 is H, F, Cl, Br, NO2 or an aliphatic acyl radical with 2 to 5 C atoms, R4 is H, halogen, OCH3, an alkyl radical with 1 to 4 C atoms or a possibly substituted aryl radical, R5 is H or a conventional functional group for producing oligonucleotides, R6 is H, OH, halogen or XR8, where X is O or S and R8 is a conventional protective group in nucleotide chemistry, B is adenine, cytosin, guanine, thymine, uracil, 2,6-diaminopurin-9-yl, hypoxanthin-9-yl, 5-methylcytosin-1-yl, 5-amino-4-imidazol carboxylic acid amid-1-yl or 5-amino-4-imidazol carboxylic acid amide-3-yl, where, if B is adenine, cytosin or guanine, the primary amino function may have a permanent protective group. These derivatives may be used for the light-controlled synthesis of oligonucleotides on a DNA chip.
专利号:EP-1112281-B1 优先权日:1998-09-08 标 题:Pteridine nucleotide analogs 发明人:HAWKINS MARY E; PFLEIDERER WOLFGANG; BALIS FRANK 权利人:US GOV HEALTH & HUMAN SERV 摘要:The invention provides pteridine nucleotides of formula (I) which are highly fluorescent and which can be used in the chemical synthesis of fluorescent oligonucleotide. The invention further provides for fluorescent oligonucleotide comprising one or more pteridine nucleotides. In addition the invention provides for pteridine nucleotide triphosphates which may be used as the constituent monomers in DNA amplification procedures. The pteridine nucleotides are more stable and possess higher quantum yields than structurally similar pteridine nucleotides.
专利号:US-5763599-A 优先权日:1994-12-16 标题:Nucleoside derivatives with photolabile protective groups 发明人:PFLEIDERER WOLFGANG; GIEGRICH HEINER 权利人:PFLEIDERER WOLFGANG 摘要:The invention relates to nucleoside derivatives having photolabile protective groups of the general formula (I) ##STR1## in which R 1 â•?H, NO 2 , CN, OCH 3 , halogen or alkyl or alkoxyalkyl having 1 to 4 C atoms n R 2 â•?H, OCH 3 n R 3 â•?H, F, Cl, Br, NO 2 n R 4 â•?H, halogen, OCH 3 , or an alkyl radical having 1 to 4 C atoms n R 5 â•?H or a usual functional group for preparing oligonucleotides n R 6 â•?H, OH, halogen or XR 8 , where Xâ•?O or S and R 8 represents a protective group usual in nucleotide chemistry, n B=adenine, cytosine, guanine, thymine, uracil, 2,6-diaminopurin-9-yl, hypoxanthin-9-yl, 5-methylcytosin-1-yl, 5-amino-4-imidazolcarboxamid-1-yl, or 5-amino-4-imidazolcarboxamid-3-yl, where in the case of B=adenine, cytosine or guanine, the primary amino function optionally exhibits a permanent protective group. n These derivatives may be used for the light-controlled synthesis of oligonucleotides on a DNA chip.
专利号:US-6716971-B1 优先权日:1998-09-08 标题:Pteridine nucleotide analogs 发明人:HAWKINS MARY E; PFLEIDERER WOLFGANG; BALIS FRANK 权利人:US HEALTH 摘要:The invention provides pteridine nucleotides of formula (I) which are highly fluorescent and which can be used in the chemical synthesis of fluorescent oligonucleotide. The invention further provides for fluorescent oligonucleotide comprising one or more pteridine nucleotides. In addition the invention provides for pteridine nucleotide triphosphates which may be used as the constituent monomers in DNA amplification procedures. The pteridine nucleotides are more stable and possess higher quantum yields than structurally similar pteridine nucleotides.
专利号:RU-2203885-C2 优先权日:2001-08-08 标题:Method of synthesis of para-aminobenzoic acid ethyl ester
[参考文献]: Neil R Hartman, Et Al. More Methemoglobin Is Produced By Benzocaine Treatment Than Lidocaine Treatment In Human In Vitro Systems. Regul Toxicol Pharmacol. 2014 Oct;70(1):182-8.
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