Potassium Carbonate → N,N-Diethyl-6-methyl-2-(4-pyridinyl)-4-pyrimidinamine

HRID 236678

反応式

HRID 236678 の反応式
ClC1C=C(C)N=C(C2C=CN=CC=2)N=1.Cl.C(NCC)C.C(=O)([O-])[O-].[K+].[K+].Cl.Cl.[CH2:29]([N:31]([CH2:45][CH3:46])[C:32]1[CH:37]=[C:36]([CH3:38])[N:35]=[C:34]([C:39]2[CH:44]=[CH:43][N:42]=[CH:41][CH:40]=2)[N:33]=1)[CH3:30]>O.C(O)C>[CH2:45]([N:31]([CH2:29][CH3:30])[C:32]1[CH:37]=[C:36]([CH3:38])[N:35]=[C:34]([C:39]2[CH:44]=[CH:43][N:42]=[CH:41][CH:40]=2)[N:33]=1)[CH3:46]

参加物

7

反応物 4

HCID 11430Potassium CarbonateHCID 10197650Diethylammonium chlorideHCID 127647054-Chloro-6-methyl-2-(pyridin-4-yl)pyrimidineHCID 12764719N,N-diethyl-6-methyl-2-(4-pyridinyl)-4-pyrimidinamine dihydrochloride

生成物 1

HCID 12764718N,N-Diethyl-6-methyl-2-(4-pyridinyl)-4-pyrimidinamine

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

A mixture containing 8.2 g. of 4-chloro-6-methyl-2-(4-pyridinyl)pyrimidine, 8.7 g. of diethylamine hydrochloride, 100 ml. of ethanol, 6 g. of potassium carbonate and 10 ml. of water was refluxed with stirring for eight hours and then concentrated in vacuo to dryness. The residue was swirled in water and the solid collected. The solid was dissolved in boiling isopropyl alcohol, the hot solution treated with decolorizing charcoal and filtered, and the hot filtrate allowed to cool. The filtrate was then saturated with gaseous hydrogen chloride, ether was added to turbidity and the mixture was allowed to stand. The separated solid was collected and dried in vacuo at 80° C. to yield 7.4 g. of N,N-diethyl-6-methyl-2-(4-pyridinyl)-4-pyrimidinamine dihydrochloride, m.p. 205°-208° C.

後処理

  1. additionA mixture containing 8.2 g
  2. concentrationconcentrated in vacuo to dryness
  3. customthe solid collected
  4. dissolutionThe solid was dissolved
  5. additionthe hot solution treated with decolorizing charcoal
  6. filtrationfiltered
  7. temperatureto cool
  8. additionsaturated with gaseous hydrogen chloride, ether was added to turbidity
  9. customThe separated solid was collected
  10. customdried in vacuo at 80° C.
  11. customto yield 7.4 g

出典と根拠

ORDレコード
ord-179b9f13f14640e5ba8919e1c2e7dc77
出典データセット
uspto-grants-1979_06
特許番号
USRE030024

関連ノート

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