반응 #1549

ord-c771bb9653f84a339085fb2d456f388e

반응 방정식

C#CCn1c(-c2ccccc2)nc(Cl)c(C)c1=O
6-chloro-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone
CNC
dimethylamine
C#CCn1c(-c2ccccc2)nc(N(C)C)c(C)c1=O
compound 23
C#CCn1c(-c2ccccc2)nc(N(C)C)c(C)c1=O
6-dimethylamino-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도to warm
  2. 2
    workup.ADDITIONafter each addition
  3. 3
    기타The solvent was removed in vacuo
  4. 4
    세척washed twice with water
  5. 5
    건조The organic layer was dried over MgSO4
  6. 6
    농축concentrated
  7. 7
    기타to yield 1.15 g crude solid product

실험 절차

To an ice cooled solution of 1.5 g (3.8 mmol) 6-chloro-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone in 4 mL of tetrahydrofuran, was added 22 mL (99 mmol) of 4.5M dimethylamine in ether portionwise (2-4 mL) over a period of 7 days. The reaction mixture was allowed to warm and stir at room temperature after each addition. The progress of the reaction was followed by gas chromatography and proceeded to 80% completion. The solvent was removed in vacuo and the residue was taken up in ether and washed twice with water. The organic layer was dried over MgSO4 and concentrated to yield 1.15 g crude solid product. Flash column chromatography on silica gel (gradient elution 25-30% ethyl acetate-hexane) afforded pure 6-dimethylamino-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone (compound 23), as a white solid. 1H-NMR (CDCl3) δ 2.2(3H,s); 2.35(1H,t); 3.5(6H,s); 4.6(2H,d); 7.65(3H,m); 7.75(2H,m).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05726124uspto-grants-1998_03