반응 #51622

ord-18dc1b1303554bae98f7737b5b480d71

반응 방정식

COc1cc2ncc(C=O)nc2cc1OC
6,7-dimethoxy-2-quinoxaline carboxaldehyde
CO.ClCCCl
MeOH 1,2-dichloroethane
NC1CCCCC1
cyclohexylamine
[BH4-].[Na+]
NaBH4
COc1cc2ncc(CNC3CCCCC3)nc2cc1OC
Cyclohexyl-(6,7-dimethoxyquinoxalin-2-ylmethyl)-amine

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGthe reaction mixture is stirred overnight
  2. 2
    농축The mixture is then concentrated
  3. 3
    기타chromatographed (50% EtOAc/hexanes—approximately 5% MeOH in 50% EtOAc/hexanes)
  4. 4
    workup.DISSOLUTIONThe oil is dissolved in EtOAc/hexanes
  5. 5
    workup.ADDITIONtreated with HCl in EtOH
  6. 6
    농축The resulting solution is concentrated
  7. 7
    기타the solids are triturated with isopropanol
  8. 8
    기타to provide a white solid
  9. 9
    기타after drying in vacuo at 60° C. (m.p. 185-190° C., dec.)

실험 절차

To a 0.067 M solution of 6,7-dimethoxy-2-quinoxaline carboxaldehyde in 2:1 MeOH/1,2-dichloroethane (7.5 mL, 0.5 mmol) is added cyclohexylamine (0.11 mL, 0.9 mmol). The reaction is allowed to stir at room temperature overnight, then NaBH4 (0.038 g, 1 mmol) is added and the reaction mixture is stirred overnight. The mixture is then concentrated and chromatographed (50% EtOAc/hexanes—approximately 5% MeOH in 50% EtOAc/hexanes). The oil is dissolved in EtOAc/hexanes and treated with HCl in EtOH. The resulting solution is concentrated and the solids are triturated with isopropanol to provide a white solid after drying in vacuo at 60° C. (m.p. 185-190° C., dec.). Anal. Calcd. for C17H23N3O2.HCl: C, 60.44; H, 7.16; N, 12.44; Found: C, 60.48; H, 6.88; N, 12.07.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06852712B2uspto-grants-2005_02