Methyl iodide → 2-Chloro-9-cyclopentyl-7,7-difluoro-5-methyl-8,9-dihydro-5H-pyrimido[4,5-B][1,4]diazepin-6(7H)-one

HRID 1880990Notes

Reaction equation

HRID 1880990 reaction equation
[Cl:1][C:2]1[N:3]=[CH:4][C:5]2[NH:6][C:7](=[O:20])[C:8]([F:19])([F:18])[CH2:9][N:10]([CH:13]3[CH2:17][CH2:16][CH2:15][CH2:14]3)[C:11]=2[N:12]=1.[H-].[Na+].[CH3:23]I>CC(N(C)C)=O>[Cl:1][C:2]1[N:3]=[CH:4][C:5]2[N:6]([CH3:23])[C:7](=[O:20])[C:8]([F:18])([F:19])[CH2:9][N:10]([CH:13]3[CH2:14][CH2:15][CH2:16][CH2:17]3)[C:11]=2[N:12]=1

Participants

5

Procedure

2-Chloro-9-cyclopentyl-7,7-difluoro-8,9-dihydro-5H-pyrimido[5,4-b][1,4]diazepin-6(7H)-one (550 mg, 1.82 mmol) was dissolved in DMA (10 mL) and cooled in an ice bath. Sodium hydride (80 mg of 60% in mineral oil, 2 mmol) was added slowly and left to stir for 10 minutes. Methyl iodide (0.125 mL, 2 mmol) was then added and the reaction mixture was warmed up to room temperature. After 30 minutes the reaction was deemed complete by LCMS, poured into ice water, the solution extracted with EtOAc. The organic layer washed with brine and water, dried over MgSO4, and concentrated to give a brown residue which was used directly for next step. [M+H] calc'd for C13H15ClF2N4O, 317; found 317.

Workup

  1. temperaturecooled in an ice bath
  2. waitleft
  3. waitAfter 30 minutes the reaction was deemed complete by LCMS
  4. extractionthe solution extracted with EtOAc
  5. washThe organic layer washed with brine and water
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated
  8. customto give a brown residue which

Sources & evidence

ORD record
ord-3dbe3f8eaf14431abc4d58165de838cc
Source dataset
uspto-grants-2012_11
Patent number
US08318727B2

Reaction notes

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