Phosgene → HCID 22063415, compound

HRID 574971Notes

Reaction equation

HRID 574971 reaction equation
[C:1](Cl)(Cl)=[O:2].C([N:7](C(C)C)C(C)C)C.[NH:14]1[CH2:19][CH2:18][CH:17]([C:20]#[N:21])[CH2:16][CH2:15]1>ClCCl>[C:20]([CH:17]1[CH2:18][CH2:19][N:14]([C:1]([NH2:7])=[O:2])[CH2:15][CH2:16]1)#[N:21]

Participants

5

Procedure

A round bottom flask containing phosgene (20% wt in toluene, 3.16 mL) and dichloromethane (10 mL) was cooled with an ice bath. A solution of N-ethyl-N-isopropylpropan-2-amine (1.385 mL) and piperidine-4-carbonitrile (0.441 g) in dichloromethane (5 mL) was added via a syringe dropwise. The mixture was stirred overnight and then concentrated to dryness. The residue was dissolved in methanol (10 mL) and 2 ml of 7 N NH3 in methanol. The mixture was stirred at 50° C. overnight. The mixture was concentrated and the residual solid was mixed with brine (5 mL) and extracted with ethyl acetate (8×25 mL). The organic solution was dried (MgSO4), filtered and concentrated. The crude material was purified on a silica gel column eluting with 5% and 10% methanol in CH2Cl2 to provide the title compound.

Workup

  1. temperaturewas cooled with an ice bath
  2. concentrationconcentrated to dryness
  3. dissolutionThe residue was dissolved in methanol (10 mL)
  4. stirringThe mixture was stirred at 50° C. overnight
  5. concentrationThe mixture was concentrated
  6. additionthe residual solid was mixed with brine (5 mL)
  7. extractionextracted with ethyl acetate (8×25 mL)
  8. dry with materialThe organic solution was dried (MgSO4)
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customThe crude material was purified on a silica gel column
  12. washeluting with 5% and 10% methanol in CH2Cl2

Sources & evidence

ORD record
ord-6de8ce14e89c4456a71ea2c4f03ef29b
Source dataset
uspto-grants-2015_05
Patent number
US09034875B2

Reaction notes

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