Dimethylformamide → 7,8-Dimethoxy-4-amino-2-[4-(2-furoyl)piperazin-1-yl]quinazoline

HRID 1703387

反応式

HRID 1703387 の反応式
[CH3:1][O:2][C:3]1[C:4]([NH2:13])=[C:5]([CH:8]=[CH:9][C:10]=1[O:11][CH3:12])[C:6]#[N:7].C[N:15](C)C=O.Cl.[O:20]1[CH:24]=[CH:23][CH:22]=[C:21]1[C:25]([N:27]1[CH2:32][CH2:31][N:30]([C:33](=N)OCC)[CH2:29][CH2:28]1)=[O:26].[H-].[Na+]>O>[CH3:12][O:11][C:10]1[C:3]([O:2][CH3:1])=[C:4]2[C:5]([C:6]([NH2:15])=[N:7][C:33]([N:30]3[CH2:31][CH2:32][N:27]([C:25]([C:21]4[O:20][CH:24]=[CH:23][CH:22]=4)=[O:26])[CH2:28][CH2:29]3)=[N:13]2)=[CH:8][CH:9]=1

参加物

6

実験手順

To a stirred solution of 1.78 g. (0.01 mole) 3,4-dimethoxy-2-aminobenzonitrile in 30 ml. of N,N-dimethylformamide is added 2.88 g. (0.01 mole) ethyl 4-(2-furoyl)piperazin-1-ylformimidate hydrochloride followed by 855 mg. (0.02 mole) of a 56.1% dispersion of sodium hydride in mineral oil. The reaction mixture is stirred at ambient temperature for 30 minutes, and then it is heated to ca. 100° C. and maintained at that temperature for 12 hours. The reaction mixture is cooled to ambient temperature, diluted with an excess of water, and then extracted with chloroform. The chloroform extract is washed several times with water, dried using anhydrous magnesium sulfate, and then evaporated to dryness in vacuo. This affords crude 7,8-dimethoxy-4-amino-2-[4-(2-furoyl)piperazin-1-yl]quinazoline, which is purified further by recrystallization from aqueous ethanol.

後処理

  1. temperatureit is heated to ca. 100° C.
  2. temperaturemaintained at that temperature for 12 hours
  3. temperatureThe reaction mixture is cooled to ambient temperature
  4. extractionextracted with chloroform
  5. extractionThe chloroform extract
  6. washis washed several times with water
  7. customdried
  8. customevaporated to dryness in vacuo

出典と根拠

ORDレコード
ord-662e012e42b440e49cc52795ac9bde36
出典データセット
uspto-grants-1982_09
特許番号
US04351940

関連ノート

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