Triethylamine → HCID 21477601, compound

HRID 864394Notes

Reaction equation

HRID 864394 reaction equation
[CH3:1][C:2]([CH3:23])([O:4][C:5]([N:7]1[CH2:12][CH2:11][N:10]([C:13]2[N:18]=[CH:17][N:16]=[C:15](Cl)[C:14]=2[N+:20]([O-])=O)[CH2:9][CH2:8]1)=[O:6])[CH3:3].C(N(CC)CC)C.[H][H]>[Pd].C(O)C>[CH3:3][C:2]([CH3:23])([O:4][C:5]([N:7]1[CH2:8][CH2:9][N:10]([C:13]2[N:18]=[CH:17][N:16]=[CH:15][C:14]=2[NH2:20])[CH2:11][CH2:12]1)=[O:6])[CH3:1]

Participants

6

Procedure

A mixture of 1-[1,1-dimethylethoxycarbonyl]-4-[4-chloro-5-nitro-6-pyrimidyl]piperazine (PREPARATION 23, 0.56 g) and triethylamine (0.3 ml) and palladium on carbon (5%, 0.13 g) in ethanol (100 ml) is charged with hydrogen gas (30 psi). After the theoretical amount of hydrogen gas is consumed, the catalyst is removed under reduced pressure. The filtrate is concentrated under reduced pressure to a foam which is diluted with an aqueous saturated solution of potassium carbonate and dichloromethane. The phases are separated and the organic phase is dried over sodium sulfate and concentrated to give to give the title compound, NMR (CDCl3) 1.49, 3.49, 3.29, 3.56, 7.98, and 8.39δ.

Workup

  1. customAfter the theoretical amount of hydrogen gas is consumed
  2. customthe catalyst is removed under reduced pressure
  3. concentrationThe filtrate is concentrated under reduced pressure to a foam which
  4. additionis diluted with an aqueous saturated solution of potassium carbonate and dichloromethane
  5. customThe phases are separated
  6. dry with materialthe organic phase is dried over sodium sulfate
  7. concentrationconcentrated
  8. customto give

Sources & evidence

ORD record
ord-17b9fce27bbb4594a1780df6322afe6d
Source dataset
uspto-grants-1996_10
Patent number
US05563142

Reaction notes

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