反应 #742308

ord-d54b4eb33b0c4bd49354dd0216ad804c

反应方程式

NCC(c1ccc(O)cc1)c1ccc(O)cc1
4,4′-(2-aminoethylidene)bis-phenol
NCC(c1ccc(O)cc1)c1ccc(O)cc1
4,4′-(2-aminoethylidene)bisphenol
O[C@@H]1[C@H](O)[C@@H](c2nnn(Cc3ccccc3)n2)O[C@H]1n1cnc2c(NCC(c3ccccc3)c3ccccc3)nc(Cl)nc21
(2R,3S,4R,5R)-2-(2-benzyl-2H-tetrazol-5-yl)-5-[2-chloro-6-(2,2-diphenyl-ethylamino)-purin-9-yl]-tetrahydro-furan-3,4-diol
NCC(c1ccc(O)cc1)c1ccc(O)cc1
Intermediate A
NCC(c1ccc(O)cc1)c1ccc(O)cc1
4,4′-(2-aminoethylidene)bisphenol
Oc1ccc(C(CNc2nc(Cl)nc3c2ncn3[C@@H]2O[C@H](c3nnn(Cc4ccccc4)n3)[C@@H](O)[C@H]2O)c2ccc(O)cc2)cc1
title compound
Oc1ccc(C(CNc2nc(Cl)nc3c2ncn3[C@@H]2O[C@H](c3nnn(Cc4ccccc4)n3)[C@@H](O)[C@H]2O)c2ccc(O)cc2)cc1
(2R,3S,4R,5R)-2-(2-Benzyl-2H-tetrazol-5-yl)-5-{6-[2,2-bis-(4-hydroxy-phenyl)ethylamino]-2 chloro-purin-9-yl}tetrahydro-furan-3,4-diol

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

The title compound is prepared in an analogous fashion to (2R,3S,4R,5R)-2-(2-benzyl-2H-tetrazol-5-yl)-5-[2-chloro-6-(2,2-diphenyl-ethylamino)-purin-9-yl]-tetrahydro-furan-3,4-diol (WO 99/38877) by replacing 2,2-diphenylethylamine with 4,4′-(2-aminoethylidene)bis-phenol (Intermediate A).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08071565B2uspto-grants-2011_12