Piperazine → HCID 20086571, compound

HRID 1608509Notes

Reaction equation

HRID 1608509 reaction equation
[C:1]([O:4][C:5]1[C:6]([CH3:21])=[C:7]([CH3:20])[C:8]2[O:13][C:12]([CH3:17])([C:14]([OH:16])=O)[CH2:11][CH2:10][C:9]=2[C:18]=1[CH3:19])(=[O:3])[CH3:2].[C:22]([N:29]1[CH:33]=[CH:32][N:31]=[CH:30]1)(N1C=CN=C1)=O.N1CCNCC1>ClC(Cl)C>[C:1]([O:4][C:5]1[C:6]([CH3:21])=[C:7]([CH3:20])[C:8]2[O:13][C:12]([C:14]([N:29]3[CH2:33][CH2:32][NH:31][CH2:30][CH2:22]3)=[O:16])([CH3:17])[CH2:11][CH2:10][C:9]=2[C:18]=1[CH3:19])(=[O:3])[CH3:2]

Participants

5

Reactant 3

HCID 4837PiperazineHCID 682631,1'-CarbonyldiimidazoleHCID 10469565HCID 10469565, compound

Product 1

HCID 20086571HCID 20086571, compound

Reagents, catalysts & solvents 1

HCID 63651,1-DichloroethaneSolvent

Procedure

2.7 g (0. 009 mol) of 3,4-dihydro-6-acetoxy-2,5,7,8-tetramethyl-2H-1-benzopyran-2-carboxylic acid are dissolved in 200 cm3 of anhydrous dichloroethane. 1 eq of carbonyldiimidazole (0.009 mol), i.e. 1.5 g, is added. The mixture is left to stir for 1 h and then 7.5 g of piperazine (0.009 mol) dissolved in 200 cm3 of dichlorcethane are added. The oil obtained after evaporation is purified on a silica column by eluting with a CH2Cl2 /ethanol/NH4OH (88/10/2) mixture and crystallized from isopropyl ether.

Workup

  1. waitThe mixture is left
  2. additionare added
  3. customThe oil obtained
  4. customafter evaporation
  5. customis purified on a silica column
  6. washby eluting with a CH2Cl2 /ethanol/NH4OH (88/10/2) mixture
  7. customcrystallized from isopropyl ether

Sources & evidence

ORD record
ord-66a15d2cd23e4ab980d18cf43034cf7c
Source dataset
uspto-grants-1995_03
Patent number
US05395834

Reaction notes

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