Posizolid, AZD-2563

泼斯唑来Chemical Name: 3-[4-[1-[2(S),3-Dihydroxypropionyl]-1,2,3,6-tetrahydropyridin-4-yl]-3,5-difluorophenyl]-5(R)-(isoxazol-3-yloxymethyl)oxazolidin-2-one
CAS No. 252260-02-9, 252260-00-7 (diastereomer)
项目整合开发状态: Discontinued
项目研究机构: AstraZeneca (Originator)
合成路线:The condensation of the protected 3,5-difluoroaniline (I) with 1-benzyl-4-piperidone (II) by means of BuLi in THF gives 4-(1-benzyl-4-hydroxypiperidin-4-yl)-3,5-difluoroaniline (III),which is dehydrated with refluxing conc.HCl to yield the tetrahydropyridine (IV).The reaction of (IV) with benzyl chloroformate in acetone/water affords the carbamate (V),which is cyclized with (R)-glycidyl butyrate (VI) by means of BuLi in THF to provide the oxazolidinone (VII).The condensation of (VII) with isoxazol-3-ol (VIII) by means of PPh3 and DIAD in THF gives the expected ether adduct (IX),which is debenzylated by reaction with 1-chloroethyl chloroformate in dichloromethane,yielding the free tetrahydropyridine derivative (X).The condensation of (X) with (S)-2,3-O-isopropylideneglyceric acid (XI) by means of DEC or DCC and TEA in dichloromethane affords the corresponding acyl tetrahydropyridine (XII),which is finally deprotected with HCl in THF to provide the target dihydroxy compound.
📌 参考资料/链接:
参考文献标题:Oxazolidinone derivs.,process for their preparation and pharmaceutical compsns.containing them
文献作者:Gravestock,M.B.(AstraZeneca plc)
参考来源:EP 1082323; JP 2002517498; WO 9964417

📄 详细内容


合成路线:The condensation of the protected 3,5-difluoroaniline (I) with 1-benzyl-4-piperidone (II) by means of BuLi in THF gives 4-(1-benzyl-4-hydroxypiperidin-4-yl)-3,5-difluoroaniline (III),which is dehydrated with refluxing conc.HCl to yield the tetrahydropyridine (IV).The reaction of (IV) with benzyl chloroformate in acetone/water affords the carbamate (V),which is cyclized with (R)-glycidyl butyrate (VI) by means of BuLi in THF to provide the oxazolidinone (VII).The condensation of (VII) with isoxazol-3-ol (VIII) by means of PPh3 and DIAD in THF gives the expected ether adduct (IX),which is debenzylated by reaction with 1-chloroethyl chloroformate in dichloromethane,yielding the free tetrahydropyridine derivative (X).The condensation of (X) with (S)-2,3-O-isopropylideneglyceric acid (XI) by means of DEC or DCC and TEA in dichloromethane affords the corresponding acyl tetrahydropyridine (XII),which is finally deprotected with HCl in THF to provide the target dihydroxy compound.
参考文献标题:Chemical processes and intermedies
文献作者:Gravestock,M.B.; Warren,K.E.H.; Ennis,D.S.; Currie,A.C.; Ainge,D.(AstraZeneca AB; AstraZeneca plc)
参考来源:WO 0140236


产品链接: CAS No. 252260-02-9››