1-Phenylpiperazine → HCID 12941113, compound

HRID 1156648Notes

Reaction equation

HRID 1156648 reaction equation
Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]([NH:9][C:10]1[CH:15]=[CH:14][C:13]([OH:16])=[CH:12][CH:11]=1)=[O:8].[C:17]1([N:23]2[CH2:28][CH2:27][NH:26][CH2:25][CH2:24]2)[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.C(N(CC)CC)C>C(O)C>[OH:16][C:13]1[CH:14]=[CH:15][C:10]([NH:9][C:7](=[O:8])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][N:26]2[CH2:27][CH2:28][N:23]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[CH2:24][CH2:25]2)=[CH:11][CH:12]=1

Participants

5

Reactant 3

HCID 70961-PhenylpiperazineHCID 8471TriethylamineHCID 12941115HCID 12941115, compound

Product 1

HCID 12941113HCID 12941113, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A solution of 45.7 g (0.16 mol) of 6-bromo-N-(4-hydroxyphenyl)hexanamide, 26.0 g (0.16 mol) of 1-phenylpiperazine and 22.4 ml (16.3 g, 0.16 mol) of triethylamine in 400 ml of ethanol was heated under reflux overnight and then concentrated under vacuum. The residue was mixed with sodium bicarbonate solution and trichloromethane. The resulting suspension was filtered. The solid was recrystallized from ethanol-water and then from acetonitrile to give the end product as tan crystals, mp 157°-159°.

Workup

  1. temperatureunder reflux overnight
  2. concentrationconcentrated under vacuum
  3. additionThe residue was mixed with sodium bicarbonate solution and trichloromethane
  4. filtrationThe resulting suspension was filtered
  5. customThe solid was recrystallized from ethanol-water

Sources & evidence

ORD record
ord-48dd01b179d34a80a8bbcf40a84c854e
Source dataset
uspto-grants-1982_06
Patent number
US04336382

Reaction notes

Loading…