Cyanamide → HCID 178512570, compound

HRID 24793Notes

Reaction equation

HRID 24793 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8]/[C:9](=[C:16]2\[C:17](=[O:25])[NH:18][C:19]3[C:24]\2=[CH:23][CH:22]=[CH:21][CH:20]=3)/[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:4][CH:3]=1.[N:26]#[C:27][NH2:28]>O1CCOCC1.Cl>[NH:1]([C:2]1[CH:7]=[CH:6][C:5]([NH:8]/[C:9](=[C:16]2\[C:17](=[O:25])[NH:18][C:19]3[C:24]\2=[CH:23][CH:22]=[CH:21][CH:20]=3)/[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:4][CH:3]=1)[C:27]([NH2:28])=[NH:26]

Participants

4

Reactant 2

HCID 9864CyanamideHCID 178507732HCID 178507732, compound

Product 1

HCID 178512570HCID 178512570, compound

Reagents, catalysts & solvents 1

HCID 204431481,4-Dioxane hydrochlorideSolvent

Procedure

Prepared analogously to Example 71 from (Z)-3-[1-(4-aminophenylamino)-1-phenyl-methylidene]-2-indolinone and cyanamide in dioxane/hydrogen chloride.

Sources & evidence

ORD record
ord-93d06ea8628549dfb80e7b37e74055e9
Source dataset
uspto-grants-2005_02
Patent number
US06855710B2

Reaction notes

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