Morpholine → HCID 23144481, compound

HRID 2238755Notes

Reaction equation

HRID 2238755 reaction equation
[CH3:1][C:2]1[N:7]=[C:6]([C:8]([C:10]2[S:14][C:13]([NH2:15])=[N:12][C:11]=2[C:16]2[O:17][CH:18]=[CH:19][CH:20]=2)=[O:9])[CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.Br[CH2:29][C:30](Br)=[O:31].[NH:33]1[CH2:38][CH2:37][O:36][CH2:35][CH2:34]1>C1COCC1.O>[O:17]1[CH:18]=[CH:19][CH:20]=[C:16]1[C:11]1[N:12]=[C:13]([NH:15][C:30](=[O:31])[CH2:29][N:33]2[CH2:38][CH2:37][O:36][CH2:35][CH2:34]2)[S:14][C:10]=1[C:8]([C:6]1[CH:5]=[CH:4][CH:3]=[C:2]([CH3:1])[N:7]=1)=[O:9]

Participants

7

Reactant 4

HCID 8083MorpholineHCID 8471Triethylamine2×HCID 61147Bromoacetyl bromideHCID 23144459HCID 23144459, compound

Product 1

HCID 23144481HCID 23144481, compound

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 8028TetrahydrofuranSolvent2×

Procedure

Compound 286 (150 mg, 0.526 mmol) and triethylamine (0.367 mL, 2.63 mmol) were dissolved in THF (4 mL), and bromoacetyl bromide (0.206 mL 2.37 mmol) was added thereto at 0° C., followed by stirring for 1 hour at room temperature. Further, a solution (2 mL) of morpholine (0.689 mL, 7.89 mmol) and triethylamine (1.10 mL, 7.89 mmol) in THF was added thereto at 0° C., followed by stirring for 1 hour at room temperature. Water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate, and then the solvent was distilled away under reduced pressure. The resulting residue was purified through silica gel column chromatography to afford the entitled Compound-287 (150 mg, 69%).

Workup

  1. customat 0° C.
  2. customat 0° C.
  3. stirringby stirring for 1 hour at room temperature
  4. extractionfollowed by extraction with ethyl acetate
  5. washThe organic layer was washed with a saturated aqueous solution of sodium chloride
  6. dry with materialdried over anhydrous magnesium sulfate
  7. distillationthe solvent was distilled away under reduced pressure
  8. customThe resulting residue was purified through silica gel column chromatography
  9. customto afford the entitled Compound-287 (150 mg, 69%)

Sources & evidence

ORD record
ord-1fa81543f6a94a0eaf4006afee67d6c7
Source dataset
uspto-grants-2010_05
Patent number
US07718808B2

Reaction notes

Loading…