Triethylamine → HCID 21890411, compound

HRID 721467Notes

Reaction equation

HRID 721467 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[C:22]([CH3:23])=[CH:21][C:19]([NH2:20])=[C:18]([CH3:24])[CH:17]=1.C([N:27](CC)CC)C.[C:32](Cl)(Cl)=[S:33].[CH2:36]([N:40]([CH2:45][CH2:46][CH2:47][CH3:48])[CH2:41][CH:42](N)[CH3:43])[CH2:37][CH2:38][CH3:39]>CN(C)C=O.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[C:22]([CH3:23])=[CH:21][C:19]([NH:20][C:32]([NH:27][CH2:43][CH2:42][CH2:41][N:40]([CH2:36][CH2:37][CH2:38][CH3:39])[CH2:45][CH2:46][CH2:47][CH3:48])=[S:33])=[C:18]([CH3:24])[CH:17]=1

Participants

7

Reactant 4

HCID 8471TriethylamineHCID 10040ThiophosgeneHCID 21394028N~1~,N~1~-Dibutylpropane-1,2-diamineHCID 218904214-((6,7-Dimethoxyquinolin-4-yl)oxy)-2,5-dimethylaniline

Product 1

HCID 21890411HCID 21890411, compoundYield 40%

Reagents, catalysts & solvents 2

HCID 6228DimethylformamideSolventHCID 8857Ethyl AcetateSolvent

Procedure

4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2,5-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 6 hr. Next, N,N-dibutylpropylenediamine (50 mg) was added thereto, and the mixture was further stirred at room temperature for 16 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 (34 mg, yield 40%).

Workup

  1. stirringthe mixture was further stirred at room temperature for 16 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-a7e507e20d1b4d42a93f55e0d0f5fd40
Source dataset
uspto-grants-2006_11
Patent number
US07135466B2

Reaction notes

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