1,2-Ethanediamine, N1,N1,N2-trimethyl- → HCID 86687243, compound

HRID 2282694Notes

Reaction equation

HRID 2282694 reaction equation
[C:1]([C:5]1[CH:6]=[C:7]([NH2:17])[N:8]([C:10]2[CH:15]=[CH:14][N:13]=[C:12](Cl)[N:11]=2)[N:9]=1)([CH3:4])([CH3:3])[CH3:2].[CH3:18][N:19]([CH3:24])[CH2:20][CH2:21][NH:22][CH3:23]>CC(O)C>[NH2:17][C:7]1[N:8]([C:10]2[CH:15]=[CH:14][N:13]=[C:12]([N:22]([CH3:23])[CH2:21][CH2:20][N:19]([CH3:24])[CH3:18])[N:11]=2)[N:9]=[C:5]([C:1]([CH3:4])([CH3:3])[CH3:2])[CH:6]=1

Participants

4

Reactant 2

HCID 673381,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 86687242HCID 86687242, compound

Product 1

HCID 86687243HCID 86687243, compoundYield 98.6%

Reagents, catalysts & solvents 1

HCID 3776IsopropanolSolvent

Procedure

A solution of Intermediate 140a (250 mg, 0.99 mmol) and N,N,N′-trimethylethylenediamine (0.32 mL, 2.48 mmol) in IPA (2.5 mL) was heated to 120° C. for 10 mins under microwave irradiation. The cooled reaction mixture was concentrated in vacuo and the residue was partitioned between EtOAc and water. The phases were separated and the aqueous layer was extracted with EtOAc (×2). The combined organic phase was washed with brine, dried (Na2SO4) and concentrated in vacuo to give the title compound (0.31 g, quant.) as a golden oil that was used in the next step without purification. LCMS (Method 3): Rt 2.51 min, m/z 318.3 [MH+].

Workup

  1. customThe cooled reaction mixture
  2. concentrationwas concentrated in vacuo
  3. customthe residue was partitioned between EtOAc and water
  4. customThe phases were separated
  5. extractionthe aqueous layer was extracted with EtOAc (×2)
  6. washThe combined organic phase was washed with brine
  7. dry with materialdried (Na2SO4)
  8. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-2639b33b529b42be9ef2b0f96f2e9595
Source dataset
uspto-grants-2015_09
Patent number
US09139584B2

Reaction notes

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