HCID 70204597, compound → HCID 86632084, compound

HRID 504550Notes

Reaction equation

HRID 504550 reaction equation
C(OC([N:8]1[C:16]2[C:11](=[CH:12][CH:13]=[C:14]([Cl:17])[CH:15]=2)/[C:10](=[CH:18]/[C:19]2[CH:24]=[C:23]([Cl:25])[CH:22]=[CH:21][C:20]=2[O:26][C:27]([C:30]([O:32][CH2:33][CH3:34])=[O:31])([CH3:29])[CH3:28])/[C:9]1=[O:35])=O)(C)(C)C.[Cl:36][C:37]1[CH:38]=[CH:39][C:40]([O:52][CH3:53])=[C:41]([CH:43]=[N:44][C:45]([O:47][Si](C)(C)C)=[CH2:46])[CH:42]=1>C1(C)C=CC=CC=1>[Cl:17][C:14]1[CH:15]=[C:16]2[NH:8][C:9](=[O:35])[C:10]3([CH:18]([C:19]4[CH:24]=[C:23]([Cl:25])[CH:22]=[CH:21][C:20]=4[O:26][C:27]([C:30]([O:32][CH2:33][CH3:34])=[O:31])([CH3:29])[CH3:28])[CH2:47][C:45](=[O:46])[NH:44][CH:43]3[C:41]3[CH:42]=[C:37]([Cl:36])[CH:38]=[CH:39][C:40]=3[O:52][CH3:53])[C:11]2=[CH:12][CH:13]=1

Participants

4

Reactant 2

HCID 70204597HCID 70204597, compoundHCID 86632085HCID 86632085, compound

Product 1

HCID 86632084HCID 86632084, compoundYield 10%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

In a manner similar to the method described in Example 10d, E/Z-6-chloro-3-[5-chloro-2-(1-ethoxycarbonyl-1-methyl-ethoxy)-benzylidene]-2-oxo-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester (7 g, 13.5 mmol) was reacted with 1-(5-chloro-2-methoxy-phenyl)-3-trimethylsilyoxy-2-aza-1,3-butadiene (45 mmol) in toluene to give title compound as a white solid (850 mg).

Sources & evidence

ORD record
ord-d2728764c08d486c86d6b2f39c1ed2d6
Source dataset
uspto-grants-2010_08
Patent number
US07776875B2

Reaction notes

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