CAS: 1835-11-6; 1-(4-(Benzyloxy)-3-Methoxyphenyl)Ethanone

上下游产品

3-Benzyloxy-4-Hydroxyacetophenone 21092-95-5
4-(苄氧基)-3-甲氧基苯甲酰甲基溴化物 3-Methoxy-4-Benzyloxy-α-Bromoacetophenone 1835-12-7
1-(4-(苄氧基)-3-羟基苯基)乙酮 1-[4-(Benzyloxy)-3-Hydroxyphenyl]Ethanone 21092-94-4
4-苄氧基-3-甲氧基苯甲酰乙酸 4-Benzyloxy-3-Methoxybenzoylacetic Acid 78178-58-2
1-(4-苄氧基-3-甲氧基-苯基)-2-(2-甲氧基-苯氧基)-乙酮 1-(4-(Benzyloxy)-3-Methoxyphenyl)-2-(2-Methoxyphenoxy)Ethan-1-One 22317-29-9
Ethyl (4-Benzyloxy-3-Methoxybenzoyl)Acetate 60525-32-8
香草乙酮 1-(3-Methoxy-4-Hydroxyphenyl)Ethanone 498-02-2
3,4-亚甲二氧苯乙酮 1-(Benzo[d][1,3]Dioxol-6-yl)Ethanone 3162-29-6 1-(Benzyloxy)-2-Methoxy-4-Vinylbenzene 55708-65-1 1-(3,4-Dihydroxyphenyl)Ethan-1-One 1197-09-7

Ethyl (4-Benzyloxy-3-Methoxybenzoyl)Acetate置于硫酸体系中,化学反应生成4-苄氧基-3-甲氧基苯乙酮
参考文献:Herbert,Richard B.; Jackson,Frederick B.; Nicolson,Ian T.,Journal Of The Chemical Society. Perkin Transactions I,1984,# 4,P. 825-831
标题:Herbert,Richard B.; Jackson,Frederick B.; Nicolson,Ian T.,Journal Of The Chemical Society. Perkin Transactions I,1984,# 4,P. 825-831

专利信息

专利号:US-6005103-A
优先权日:1993-11-19
标题 :Pyrone derivatives as protease inhibitors and antiviral agents
发明人：DOMAGALA JOHN MICHAEL; LUNNEY ELIZABETH; PARA KIMBERLY SUZANNE; PRASAD JOSYULA VENKATA NAGENDR; TAIT BRADLEY DEAN
权利人:WARNER LAMBERT CO
摘要:The present invention relates to novel tri- and tetrasubstituted pyrones and related structures which potently inhibit the HIV aspartyl protease blocking HIV infectivity. The pyrone derivatives are useful in the development of therapies for the treatment of bacterial and viral infections and diseases, including AIDS. The present invention is also directed to methods of synthesis of multifunctionalized pyrones and of related structures.

专利号:US-8524740-B2
优先权日:2010-07-15
标 题 :Synthesis and anticancer activity of aryl and heteroaryl-quinolin derivatives
发明人：KUO SHENG-CHU; LEE KUO-HSIUNG; HUANG LI-JIAU; CHOU LI-CHEN; WU TIAN-SHUNG; WAY TZONG-DER; CHUNG JING-GUNG; YANG JAI-SING; HUANG CHI-HUNG; TSAI MENG-TUNG
权利人:KUO SHENG-CHU; LEE KUO-HSIUNG; HUANG LI-JIAU; CHOU LI-CHEN; WU TIAN-SHUNG; WAY TZONG-DER; CHUNG JING-GUNG; YANG JAI-SING; HUANG CHI-HUNG; TSAI MENG-TUNG; TAIRX INC
摘要:A compound of Formula I is disclosed as follows: n n n n n n n n n n n n or a pharmaceutically acceptable salt, prodrug, solvate, or metabolite thereof, wherein n R is hydrogen, P(â•?O)(OH) 2 , P(â•?O)(O(C 1 -C 18 )alkylene(C 6 -C 20 )aryl) 2 , P(â•?O)(OH)(OM), P(â•?O)(OM) 2 , Pâ•?O(O 2 M), S(â•?O)(OH) 2 , S(â•?O)(O(C 1 -C 18 )alkylene(C 6 -C 20 )aryl) 2 , S(â•?O)(OH)(OM), S(â•?O)(OM) 2 ; n M is a monovalent or divalent metal ion, or alkylammonium ion; n W is (C 6 -C 20 )aryl, (C 6 -C 20 )heteroaryl, (C 1 -C 18 )alkyl(C 6 -C 20 )aryl, (C 1 -C 18 )alkyl(C 6 -C 20 )heteroaryl, hydroxy(C 6 -C 20 )aryl, hydroxy(C 6 -C 20 )heteroaryl, (C 1 -C 18 )alkoxy(C 6 -C 20 )aryl, (C 1 -C 18 )alkoxy(C 6 -C 20 )heteroaryl, (C 1 -C 18 )alkylenedioxy(C 6 -C 20 )aryl, (C 1 -C 18 )alkylenedioxy(C 6 -C 20 )heteroaryl, halo(C 6 -C 20 )aryl, halo(C 6 -C 20 )heteroaryl, (C 1 -C 18 )alkylamino(C 6 -C 20 )aryl, (C 1 -C 18 )alkylamino(C 6 -C 20 )heteroaryl, (C 1 -C 18 )cycloalkylamino(C 6 -C 20 )aryl, or (C 1 -C 18 )cycloalkylamino(C 6 -C 20 )heteroaryl, and their OR 8 substutes; n R 5 is (C 1 -C 18 alkoxy, hydrogen, hydroxyl, O—(C 1 -C 18 )alkyl(C 6 -C 20 )aryl, halo or OR 8 , or R 5 and R 6 are (C 1 -C 18 )dioxy provided that R 7 is hydrogen; n R 6 is hydroxyl, O—(C 1 -C 18 )alkyl(C 6 -C 20 )aryl, halo or OR 8 , (C 1 -C 18 )alkoxy, (C 1 -C 18 )alkylamino, or (C 1 -C 18 )cycloalkylamino, or R 6 and R 7 are (C 1 -C 18 )dioxy provided that R 5 is hydrogen; n R 7 is hydrogen, halo or OR 8 , hydroxyl, or O—(C 1 -C 18 )alkyl(C 6 -C 20 )aryl; and n R 8 is P(â•?O)(OH) 2 , P(â•?O)(O(C 1 -C 18 )alkyl(C 6 -C 20 )aryl) 2 , Pâ•?O)(OH)(OM), or P(â•?O)(OM) 2 , Pâ•?O(O 2 M).

专利号:EP-0729465-B1
优先权日:1993-11-19
标 题:Pyrone derivatives as protease inhibitors and antiviral agents
发明人：DOMAGALA JOHN MICHAEL; LUNNEY ELIZABETH; PARA KIMBERLY SUZANNE; PRASAD JOSYULA VENKATA NAGENDR; TAIT BRADLEY DEAN
权利人:PARKE DAVIS & CO
摘要:The present invention relates to novel tri- and tetrasubstituted pyrones and related structures which potently inhibit the HIV aspartyl protease blocking HIV infectivity. The pyrone derivatives are useful in the development of therapies for the treatment of bacterial and viral infections and diseases, including AIDS. The present invention is also directed to methods of synthesis of multifunctionalized pyrones and of related structures.

专利号:CA-2805590-C
优先权日:2010-07-15
标题 :Synthesis and anticancer activity of aryl and heteroaryl-quinolin derivatives

专利号:US-2012015908-A1
优先权日:2010-07-15
标 题 :Synthesis and anticancer activity of aryl and heteroaryl-quinolin derivatives

专利号:WO-2012009519-A1
优先权日:2010-07-15
标题:Synthesis and anticancer activity of aryl and heteroaryl-quinolin derivatives