Dimethylformamide → HCID 86593463, compound

HRID 721461Notes

Reaction equation

HRID 721461 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[N:9]=[CH:8][CH:7]=[C:6]2[O:15][C:16]1[CH:22]=[CH:21][C:19]([NH2:20])=[C:18]([CH3:23])[C:17]=1[CH3:24].C([N:27]([CH2:30]C)CC)C.[C:32](Cl)(Cl)=[S:33].N[CH2:37][CH2:38][CH2:39][N:40]1[CH:44]=[CH:43][N:42]=[CH:41]1.CN(C)C=[O:48]>C(OCC)(=O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[N:9]=[CH:8][CH:7]=[C:6]2[O:15][C:16]1[CH:22]=[CH:21][C:19]([NH:20][C:32]([NH:27][CH2:30][CH2:37][CH2:38][C:39]([N:40]2[CH:44]=[CH:43][N:42]=[CH:41]2)=[O:48])=[S:33])=[C:18]([CH3:23])[C:17]=1[CH3:24]

Participants

7

Reactant 5

HCID 6228DimethylformamideHCID 8471TriethylamineHCID 10040ThiophosgeneHCID 787361H-Imidazole-1-propanamineHCID 218904394-[(6,7-Dimethoxy-4-quinolyl)oxy]-2,3-dimethylaniline

Product 1

HCID 86593463HCID 86593463, compoundYield 17%

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2,3-dimethylaniline (51 mg) was dissolved in N,N-dimethylformamide (2 ml) and triethylamine (1 ml) to prepare a solution. Thiophosgene (51 mg) was then added to the solution, and the mixture was stirred at room temperature for 7 hr. Next, 1-(3-aminopropyl)imidazole (50 mg) was added thereto, and the mixture was further stirred at room temperature for 13 hr. Ethyl acetate was added to the reaction solution, followed by washing with water and saturated brine in that order. The organic layer was then dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by HPLC using chloroform/methanol for development to give the title compound (13 mg, yield 17%).

Workup

  1. stirringthe mixture was further stirred at room temperature for 13 hr
  2. washby washing with water and saturated brine in that order
  3. dry with materialThe organic layer was then dried over anhydrous sodium sulfate
  4. customThe solvent was removed by distillation under the reduced pressure
  5. customthe residue was purified by HPLC

Sources & evidence

ORD record
ord-8af9e87d0fb743e39b073943b2856e8b
Source dataset
uspto-grants-2006_11
Patent number
US07135466B2

Reaction notes

Loading…