Acetamidine monohydrochloride → HCID 178440130, compound

HRID 1708400Notes

Reaction equation

HRID 1708400 reaction equation
[Na].Cl.[C:3]([NH2:6])(=[NH:5])[CH3:4].[N+:7]([C:10]1[CH:27]=[CH:26][C:13]([CH2:14][CH:15]([C:21](=O)[CH2:22][CH2:23][CH3:24])[C:16](OCC)=[O:17])=[CH:12][CH:11]=1)([O-:9])=[O:8]>C(O)C>[CH2:22]([C:21]1[N:6]=[C:3]([CH3:4])[N:5]=[C:16]([OH:17])[C:15]=1[CH2:14][C:13]1[CH:12]=[CH:11][C:10]([N+:7]([O-:9])=[O:8])=[CH:27][CH:26]=1)[CH2:23][CH3:24]

Participants

5

Reactant 3

HCID 67170Acetamidine monohydrochlorideHCID 5360545SodiumHCID 9971622HCID 9971622, compound

Product 1

HCID 178440130HCID 178440130, compoundYield 55.6%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

3.5 g of sodium are dissolved in 175 ml of ethanol. 9.5 g of acetamidine hydrochloride are added to this solution and the mixture is stirred for 5 minutes at room temperature. 20 g of ethyl 2-(4-nitrobenzyl)-3-oxohexanoate, prepared in Example 3, are then added and the mixture is stirred for 4 days at room temperature. The solvents are then evaporated off under vacuum and the residue is taken up with hydrochloric acid solution and extracted with ethyl acetate. The organic phase is dried over magnesium sulphate and then evaporated under vacuum to give an oily residue which crystallises in an acetone/ether mixture. The crystals are drained and dried and give 10.9 g of 6-n-propyl-2-methyl-4-hydroxy-5-(4-nitrobenzyl)pyrimidine in the form of crystals of melting point 200° C.

Workup

  1. additionare then added
  2. stirringthe mixture is stirred for 4 days at room temperature
  3. customThe solvents are then evaporated off under vacuum
  4. extractionextracted with ethyl acetate
  5. dry with materialThe organic phase is dried over magnesium sulphate
  6. customevaporated under vacuum
  7. customto give an oily residue which
  8. customcrystallises in an acetone/ether mixture
  9. customdried

Sources & evidence

ORD record
ord-d9bc27595328438f96ce9099cb07e0cd
Source dataset
uspto-grants-1994_10
Patent number
US05358950

Reaction notes

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