反应详情

A flask was charged with 4-{(2S,4R)-1-acetyl-4-[(4-chlorophenyl)amino]-2-methyl-1,2,3,4-tetrahydro-6-quinolinyl}benzoic acid (for a preparation see example 6) (109 mg, 0.251 mmol), HOBT.NH3 (85 mg, 0.501 mmol) and EDC (57.7 mg, 0.301 mmol) then filled with dichloromethane (DCM) (5 mL) and the resulting mixture was treated with N-ethylmorpholine (NEM) (0.095 mL, 0.752 mmol) then stirred a room temperature. After 4 h, 50% of the previous quantities of EDAC, HOBT and NEM were added and the resulting mixture was stirred at room temperature for 16 h. Most of the DCM was removed in vacuo and the residue was partitioned between AcOEt and water. The layers were separated and the aqueous phase was extracted with AcOEt. The combined organic phases were washed twice with a saturated NaHCO3 aqueous solution then brine, dried over MgSO4 and concentrated in vacuo. The residue was triturated with Et2O then filtered off and dried under house vacuum to give 4-{(2S,4R)-1-acetyl-4-[(4-chlorophenyl)amino]-2-methyl-1,2,3,4-tetrahydro-6-quinolinyl}benzamide (75 mg, 0.173 mmol, 69.0% yield) as a very pale yellow solid.

1. stirringthe resulting mixture was stirred at room temperature for 16 h
2. customMost of the DCM was removed in vacuo
3. customthe residue was partitioned between AcOEt and water
4. customThe layers were separated
5. extractionthe aqueous phase was extracted with AcOEt
6. washThe combined organic phases were washed twice with a saturated NaHCO3 aqueous solution
7. dry with materialbrine, dried over MgSO4
8. concentrationconcentrated in vacuo
9. customThe residue was triturated with Et2O
10. filtrationthen filtered off
11. customdried under house vacuum