Methane → 2-Dimethylaminocarbonyl-N-[(4-methylquinazolin-2-yl)aminocarbonyl]benzenesulfonamide

HRID 1155942Notes

Reaction equation

HRID 1155942 reaction equation
C[Al](C)C.[CH3:5][NH:6][CH3:7].C.[CH3:9][C:10]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[N:13]=[C:12]([NH:20][C:21]([NH:23][S:24]([C:27]2[CH:36]=[CH:35][CH:34]=[CH:33][C:28]=2[C:29]([O:31]C)=O)(=[O:26])=[O:25])=[O:22])[N:11]=1>CCCCCC.C(Cl)Cl.C1(C)C=CC=CC=1>[CH3:5][N:6]([CH3:7])[C:29]([C:28]1[CH:33]=[CH:34][CH:35]=[CH:36][C:27]=1[S:24]([NH:23][C:21]([NH:20][C:12]1[N:11]=[C:10]([CH3:9])[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[N:13]=1)=[O:22])(=[O:25])=[O:26])=[O:31]

Participants

8

Reactant 4

HCID 297MethaneHCID 674DimethylamineHCID 14774717Methyl 2-[[(4-methylquinazolin-2-yl)aminocarbonyl]aminosulfonyl]benzoateHCID 16682925Trimethylaluminum

Product 1

HCID 205362642-Dimethylaminocarbonyl-N-[(4-methylquinazolin-2-yl)aminocarbonyl]benzenesulfonamide

Reagents, catalysts & solvents 3

HCID 1140TolueneSolventHCID 6344DichloromethaneSolventHCID 8058HexaneSolvent

Procedure

To 21.2 ml of 25% trimethylaluminum in hexane (2.36 M) in 100 ml dry methylene chloride is added 2.2 g dimethylamine. The mixture is stirred at ambient temperature until evolution of methane gas ceases and then 20.0 g of methyl 2-[[(4-methylquinazolin-2-yl)aminocarbonyl]aminosulfonyl]benzoate and 200 ml of dry toluene is added. The resulting mixture is heated to distill off the methylene chloride and hexane, after which heating is continued at the reflux temperature of toluene. After 2 hours, the toluene is removed in vacuo, and 200 ml of methylene chloride and 100 ml of 10% hydrochloric acid are added. The phases are separated, and the methylene chloride phase is washed once with water, dried over magnesium sulfate, and filtered, and the methylene chloride distilled to yield the desired compound.

Workup

  1. temperatureThe resulting mixture is heated
  2. distillationto distill off the methylene chloride and hexane
  3. temperatureafter which heating
  4. customthe toluene is removed in vacuo, and 200 ml of methylene chloride and 100 ml of 10% hydrochloric acid
  5. additionare added
  6. customThe phases are separated
  7. washthe methylene chloride phase is washed once with water
  8. dry with materialdried over magnesium sulfate
  9. filtrationfiltered
  10. distillationthe methylene chloride distilled

Sources & evidence

ORD record
ord-008275ff026e4a47a70d4c2aac3374e4
Source dataset
uspto-grants-1982_06
Patent number
US04333760

Reaction notes

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