Water → HCID 18174654, compound

HRID 395860Notes

Reaction equation

HRID 395860 reaction equation
[N:1]1[CH:6]=[CH:5][C:4]([N:7]2[CH2:12][CH2:11][CH:10]([CH2:13][NH2:14])[CH2:9][CH2:8]2)=[CH:3][CH:2]=1.[N+:15]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[CH2:24][C:25](O)=[O:26])([O-])=O.CCOC(C)=O.O>CN(C=O)C>[NH2:15][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[CH2:24][C:25]([NH:14][CH2:13][CH:10]1[CH2:9][CH2:8][N:7]([C:4]2[CH:5]=[CH:6][N:1]=[CH:2][CH:3]=2)[CH2:12][CH2:11]1)=[O:26]

Participants

6

Procedure

A solution of 1-(4-pyridyl)piperidine-4-methylamine (156 mg, 0.817 mmol), 2-nitrophenylacetic acid (159 mg, 0.875 mmol), and 1-[3-(dimethylaminopropyl]-3-ethylcarbodiimide hydrochloride (168 mg, 0.875 mmol) in DMF was stirred 16 h; and the mixture was poured into EtOAc and H2O. The aqueous layer was washed with EtOAc (2×) and the combined extracts were dried (K2CO3) and concentrated. The under an atmosphere of hydrogen gas. After 2.5 h, the mixture was filtered and the filtrate concentrated. The residue was dissolved in 5% HOAc in MeOH and loaded onto a SCX Column (Varian). The column was eluted with MeOH followed by 2 M NH3 in MeOH. The latter fractions were concentrated yielding 158.6 mg (60%) of the title compound.

Workup

  1. washThe aqueous layer was washed with EtOAc (2×)
  2. dry with materialthe combined extracts were dried (K2CO3)
  3. concentrationconcentrated
  4. filtrationthe mixture was filtered
  5. concentrationthe filtrate concentrated
  6. dissolutionThe residue was dissolved in 5% HOAc in MeOH
  7. washThe column was eluted with MeOH
  8. concentrationThe latter fractions were concentrated

Sources & evidence

ORD record
ord-f640a314ae554e258295163f81a585af
Source dataset
uspto-grants-2003_08
Patent number
US06605626B2

Reaction notes

Loading…