Hydrochloric Acid → Methyl 2-(isopropylamino)pyrimidine-5-carboxylate

HRID 374428ノート

反応式

HRID 374428 の反応式
S(O)(O)(=O)=O.[CH:6]([NH:9][C:10]([NH2:12])=[NH:11])([CH3:8])[CH3:7].N1C[CH2:16][CH2:15][CH2:14]1.[CH3:18][O:19]C(C=O)C=O.Cl.[CH3:26][OH:27]>C(OCC)(=O)C>[CH:6]([NH:9][C:10]1[N:12]=[CH:16][C:15]([C:26]([O:19][CH3:18])=[O:27])=[CH:14][N:11]=1)([CH3:8])[CH3:7]

参加物

7

実験手順

A mixture of 11.62 g (77.5 mmol) of isopropylguanidine hydrogen sulfate, 32 ml (5 eq; 0.37 mol) of freshly distilled pyrrolidine in 230 ml of anhydrous methanol is refluxed for twenty minutes. A methanolic solution (60 ml) of methoxymalonaldehyde (1 eq; 77.5 mmol; 10 g) is added to the above solution at 0° C. as well as 140 g of molecular sieve (4 A °). The reaction medium is stirred under argon and under reflux for 24 hours. The molecular sieves are removed by filtration and then rinsed with methanol. Evaporation of the filtrate gives a residue which is taken up with ethyl acetate and then acidified with a 1N hydrochloric acid solution. The organic phases are washed with a saturated sodium chloride solution, dried over sodium sulfate, evaporated and purified on silica gel under 200 mb (eluent: 50 ethyl acetate/50 heptane).

後処理

  1. temperatureis refluxed for twenty minutes
  2. temperatureunder reflux for 24 hours
  3. customThe molecular sieves are removed by filtration
  4. washrinsed with methanol
  5. customEvaporation of the filtrate
  6. customgives a residue which
  7. washThe organic phases are washed with a saturated sodium chloride solution
  8. dry with materialdried over sodium sulfate
  9. customevaporated
  10. custompurified on silica gel under 200 mb (eluent: 50 ethyl acetate/50 heptane)

出典と根拠

ORDレコード
ord-b1688e95101f450980c1e1346da528fe
出典データセット
uspto-grants-1996_01
特許番号
US05480884

反応ノート

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