HCID 22569540, compound → HCID 178505115, compound

HRID 24886Notes

Reaction equation

HRID 24886 reaction equation
C(O[C:4](=[C:11]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[NH:13][C:12]1=[O:20])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)C.[C:21]([CH2:23][N:24]([C:29]1[CH:35]=[CH:34][C:32]([NH2:33])=[CH:31][CH:30]=1)[S:25]([CH3:28])(=[O:27])=[O:26])#[N:22]>CN(C=O)C>[C:21]([CH2:23][N:24]([C:29]1[CH:35]=[CH:34][C:32]([NH:33]/[C:4](=[C:11]2\[C:12](=[O:20])[NH:13][C:14]3[C:19]\2=[CH:18][CH:17]=[CH:16][CH:15]=3)/[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=2)=[CH:31][CH:30]=1)[S:25]([CH3:28])(=[O:27])=[O:26])#[N:22]

Participants

4

Reactant 2

HCID 22569540HCID 22569540, compoundHCID 540376233-(1-Ethoxy-1-phenyl-methylidene)-2-indolinone

Product 1

HCID 178505115HCID 178505115, compound

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

Prepared analogously to Example 11 from 3-(1-ethoxy-1-phenyl-methylidene)-2-indolinone and 4-(N-cyanomethyl-N-methylsulphonyl-amino)-aniline in DMF.

Sources & evidence

ORD record
ord-23b3b5d39dbf49818da061a0fc6c8bb8
Source dataset
uspto-grants-2005_02
Patent number
US06855710B2

Reaction notes

Loading…