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

HRID 1760752노트

반응식

HRID 1760752 반응식
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]

참가 물질

6

실험 절차

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 NH4C1 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+).

후처리

  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 NH4C1 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

출처 및 근거

ORD 기록
ord-a0af2c34208d4204adf5d3c4a5b798df
출처 데이터셋
uspto-grants-2005_01
특허 번호
US06844435B2

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