A-317920
Chemical Name: N-[2-[4-[3-[4-(Cyclopropylcarbonyl)phenoxy]propyl]piperazin-1-yl]-1(R)-methyl-2-oxoethyl]furan-2-carboxamide
CAS No. 360551-59-3
项目整合开发状态: Preclinical
项目研究机构: Abbott (Originator)
合成路线:Alkylation of 4-cyano-4'-hydroxybiphenyl (I) with 1-bromo-3-chloropropane (II) yields the chloropropyl ether (III).This is then condensed with the mono-protected homopiperazine (IV) to furnish (V).Removal of the N-Boc group of (V) to afford amine (VI) is then accomplished by treatment with trifluoroacetic acid in CH2Cl2.Amine (VI) is subsequently coupled with N-Boc-D-thiazolylalanine (VII) in the presence of EDC/DMAP producing amide (VIII).(1,2)
合成路线:Acidic cleavage of the N-Boc group of (VIII) furnishes amine (IX).Finally,acylation of (IX) with 2-furoyl chloride (X) leads to the title compound.(1,2)
合成路线:Intramolecular cyclization of p-hydroxy-4-chlorobutyrophenone (I) under alkaline conditions yields cyclopropyl(4-hydroxyphenyl) ketone (II).The phenolic hydroxyl group is then alkylated by 1-bromo-3-chloropropane (III) to furnish the chloropropyl ether (IV).Subsequent condensation of alkyl chloride (IV) with piperazine (V) gives rise to the N-substituted piperazine (VI).This is then coupled with N-Boc-L-alanine (VII) in the presence of EDC/DMAP to afford amide (VIII) (1,2).After acidic cleavage of the N-Boc protecting group,the resultant monosubstituted piperazine (IX) is acylated by furanoyl chloride (X) to furnish the target furamide derivative
合成路线:Cyclization of 4-chloro-4'-hydroxybutyrophenone (I) in the presence of 50% aqueous NaOH produces cyclopropyl (4-hydroxyphenyl) ketone (II).This is then alkylated with 1-bromo-3-chloropropane (III) to afford the chloropropyl ether (IV).Chloride displacement in (IV) with an excess of piperazine (V) in the presence of KI and K2CO3 furnishes the monosubstituted piperazine (VI).Subsequent coupling of piperazine (VI) with N-Boc-L-alanine (VII) leads to amide (VIII).Finally,Boc group cleavage in (VIII) employing trifluoroacetic acid yields the title compound (1-3).
📌 参考资料/链接:
参考文献标题:Cyclic and bicyclic diamino histamine-3 receptor antagonists
文献作者:Black,L.A.; Faghih,R.; Bennani,Y.L.; Liu,H.; Zhang,H.Q.; Dwight,W.J.; Gentles,R.G.; Phelan,K.M.; Vasudevan,A.(Abbott Laboratories Inc.)
参考来源:WO 0166534
📄 详细内容
合成路线:Intramolecular cyclization of p-hydroxy-4-chlorobutyrophenone (I) under alkaline conditions yields cyclopropyl(4-hydroxyphenyl) ketone (II).The phenolic hydroxyl group is then alkylated by 1-bromo-3-chloropropane (III) to furnish the chloropropyl ether (IV).Subsequent condensation of alkyl chloride (IV) with piperazine (V) gives rise to the N-substituted piperazine (VI).This is then coupled with N-Boc-L-alanine (VII) in the presence of EDC/DMAP to afford amide (VIII) (1,2).After acidic cleavage of the N-Boc protecting group,the resultant monosubstituted piperazine (IX) is acylated by furanoyl chloride (X) to furnish the target furamide derivative
合成路线:Cyclization of 4-chloro-4'-hydroxybutyrophenone (I) in the presence of 50% aqueous NaOH produces cyclopropyl (4-hydroxyphenyl) ketone (II).This is then alkylated with 1-bromo-3-chloropropane (III) to afford the chloropropyl ether (IV).Chloride displacement in (IV) with an excess of piperazine (V) in the presence of KI and K2CO3 furnishes the monosubstituted piperazine (VI).Subsequent coupling of piperazine (VI) with N-Boc-L-alanine (VII) leads to amide (VIII).Finally,Boc group cleavage in (VIII) employing trifluoroacetic acid yields the title compound (1-3).
参考文献标题:Cyclic and bicyclic diamino histamine-3 receptor antagonists
文献作者:Black,L.A.; Faghih,R.; Bennani,Y.L.; Liu,H.; Zhang,H.Q.; Dwight,W.J.; Gentles,R.G.; Phelan,K.M.; Vasudevan,A.(Abbott Laboratories Inc.)
参考来源:US 2001049367; US 6559140
合成路线:Intramolecular cyclization of p-hydroxy-4-chlorobutyrophenone (I) under alkaline conditions yields cyclopropyl(4-hydroxyphenyl) ketone (II).The phenolic hydroxyl group is then alkylated by 1-bromo-3-chloropropane (III) to furnish the chloropropyl ether (IV).Subsequent condensation of alkyl chloride (IV) with piperazine (V) gives rise to the N-substituted piperazine (VI).This is then coupled with N-Boc-L-alanine (VII) in the presence of EDC/DMAP to afford amide (VIII) (1,2).After acidic cleavage of the N-Boc protecting group,the resultant monosubstituted piperazine (IX) is acylated by furanoyl chloride (X) to furnish the target furamide derivative
参考文献标题:Acyl-D-alanine amides: Selective histamine H3 receptor antagonists
文献作者:Black,L.A.; Faghih,R.; Liu,H.; et al.
参考来源:224th ACS Natl Meet (Aug 18 2002,Boston) 2002,Abst MEDI 323
产品链接: CAS No. 360551-59-3››