Dimethyl Sulfoxide → HCID 22936690, compound

HRID 853551Notes

Reaction equation

HRID 853551 reaction equation
C1([O:7][C:8](=O)[NH:9][C:10]2[CH:15]=[CH:14][C:13]([O:16][C:17]3[C:26]4[C:21](=[CH:22][C:23]([O:30][CH3:31])=[C:24]([C:27](=[O:29])[NH2:28])[CH:25]=4)[N:20]=[CH:19][CH:18]=3)=[CH:12][C:11]=2[CH3:32])C=CC=CC=1.CS(C)=O.[CH2:38]([NH2:40])[CH3:39].O1CCCC1>C(OCC)(=O)C.O>[C:27]([C:24]1[CH:25]=[C:26]2[C:21](=[CH:22][C:23]=1[O:30][CH3:31])[N:20]=[CH:19][CH:18]=[C:17]2[O:16][C:13]1[CH:14]=[CH:15][C:10]([NH:9][C:8]([NH:40][CH2:38][CH3:39])=[O:7])=[C:11]([CH3:32])[CH:12]=1)(=[O:29])[NH2:28]

Participants

7

Reactant 4

HCID 679Dimethyl SulfoxideHCID 6341EthylamineHCID 8028TetrahydrofuranHCID 58931269HCID 58931269, compound

Product 1

HCID 22936690HCID 22936690, compound

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 8857Ethyl AcetateSolvent

Procedure

[4-(6-carbamoyl-7-methoxy-4-quinolyl)oxy-2-methyl-phenyl]-carbamic acid phenyl ester (65 mg) was added to dimethylsulfoxide (1.0 ml), and then an ethylamine-containing 2N tetrahydrofuran solution (0.37 ml) was added and the mixture was stirred for 5 minutes. Water and ethyl acetate were added to the reaction solution, and the precipitated crystals were filtered out to obtain the title compound (38 mg).

Workup

  1. additionwas added
  2. filtrationthe precipitated crystals were filtered out

Sources & evidence

ORD record
ord-7c90add82b4546b5a31a17a83bae2a4d
Source dataset
uspto-grants-2007_08
Patent number
US07253286B2

Reaction notes

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