Benzoyl chloride → 2-(2,6-Dichlorophenylamino)-1-methyl-7-phenyl-1,8-dihydro-9H-imidazo [4,5-f]quinazoline-9-one

HRID 2296717ノート

反応式

HRID 2296717 の反応式
N[NH-].[C:3](Cl)(=O)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.C(N(CC)CC)C.[NH2:19][C:20]1[CH:38]=[CH:37][C:23]2[N:24]=[C:25]([NH:28][C:29]3[C:34]([Cl:35])=[CH:33][CH:32]=[CH:31][C:30]=3[Cl:36])[N:26]([CH3:27])[C:22]=2[C:21]=1[C:39]([NH2:41])=[O:40]>C1COCC1>[Cl:36][C:30]1[CH:31]=[CH:32][CH:33]=[C:34]([Cl:35])[C:29]=1[NH:28][C:25]1[N:26]([CH3:27])[C:22]2=[C:21]3[C:20](=[CH:38][CH:37]=[C:23]2[N:24]=1)[N:19]=[C:3]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)[NH:41][C:39]3=[O:40]

参加物

6

実験手順

The above amino amide (50 mg, 0.15 mmol) was added to a solution of benzoyl chloride (32 mg, 0.23 mmol) in THF (1 mL). Triethylamine (0.03 mL, 0.23 mmol) was added and the mixture stirred for 1 h. TLC showed conversion to the benzamide. The solvent was evaporated and the residue dissolved in MeOH (1 mL). Sodium methoxide in MeOH (25%, 0.2 mL) was added and the solution heated to reflux for 45 min. The cooled mixture was partitioned between 1M NH4Cl and CH2Cl2. The residue from the organic layer was stirred and refluxed with MeOH (2 mL) for 1 h, cooled, filtered and washed with MeOH to yield the title compound, 7 (52 mg, 79%) Mp>300° C. MS (ES+) 436,438 (MH+).

後処理

  1. customThe solvent was evaporated
  2. dissolutionthe residue dissolved in MeOH (1 mL)
  3. additionSodium methoxide in MeOH (25%, 0.2 mL) was added
  4. temperaturethe solution heated
  5. temperatureto reflux for 45 min
  6. customThe cooled mixture was partitioned between 1M NH4Cl and CH2Cl2
  7. stirringThe residue from the organic layer was stirred
  8. temperaturerefluxed with MeOH (2 mL) for 1 h
  9. temperaturecooled
  10. filtrationfiltered
  11. washwashed with MeOH

出典と根拠

ORDレコード
ord-d19ba1c0510042e9a3ec06fb226ec6d0
出典データセット
uspto-grants-2002_12
特許番号
US06489328B2

反応ノート

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