Reaction #8810

ord-d8649f47a7b846b880d52e1adecdf85c

Reaction equation

O=c1[nH]cnc2c1CCN(Cc1ccccc1)C2
7-benzyl-5,6,7,8-tetrahydro-3H-pyrido[3,4-d]pyrimidin-4-one
CCN(CC)c1ccccc1
N,N-diethylaniline
O=P(Cl)(Cl)Cl
POCl3
Clc1ncnc2c1CCN(Cc1ccccc1)C2
7-benzyl-4-chloro-5,6,7,8-tetrahydro-pyrido[3,4-d]pyrimidine

Conditions

Temperature
80°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherAfter evaporation of the excess of POCl3
  2. 2
    workup.ADDITIONthe residue was poured into ice, dichloromethane
  3. 3
    workup.ADDITIONwas added
  4. 4
    ExtractionThe product was extracted with dichloromethane
  5. 5
    Otherdried
  6. 6
    Concentrationconcentrated

Procedure

To a mixture of 7-benzyl-5,6,7,8-tetrahydro-3H-pyrido[3,4-d]pyrimidin-4-one 3a (1.0 g, 4.14 mmol) and N,N-diethylaniline (0.37 g, 2.48 mmol) was slowly added POCl3 (12 mL). The mixture was heated to 80° C. for 20 h. After evaporation of the excess of POCl3, the residue was poured into ice, dichloromethane was added and the mixture was made basic (pH=11) with solid Na2CO3. The product was extracted with dichloromethane, dried, and concentrated. Flash column chromatography with 20% ethyl acetate:hexane gave 0.46 g of 7-benzyl-4-chloro-5,6,7,8-tetrahydro-pyrido[3,4-d]pyrimidine 4a as a yellow oil.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091200B2uspto-grants-2006_08