5-chloro-1H-indole-2,3-dione → HCID 18518670, compound

HRID 1369064Notes

Reaction equation

HRID 1369064 reaction equation
Cl.[CH2:2]([N:4]([CH2:9][CH3:10])[CH2:5][CH2:6][CH2:7]Cl)[CH3:3].[Cl:11][C:12]1[CH:13]=[C:14]2[C:18](=[CH:19][CH:20]=1)[NH:17][C:16](=[O:21])[C:15]2=[O:22]>>[CH2:2]([N:4]([CH2:9][CH3:10])[CH2:5][CH2:6][CH2:7][N:17]1[C:18]2[C:14](=[CH:13][C:12]([Cl:11])=[CH:20][CH:19]=2)[C:15](=[O:22])[C:16]1=[O:21])[CH3:3]

Participants

3

Reactant 2

HCID 872035-chloro-1H-indole-2,3-dioneHCID 145749Diethylaminopropyl chloride, hydrochloride

Product 1

HCID 18518670HCID 18518670, compound

Procedure

This compound was prepared by the same method as that described in reference example 8, using 3-diethylaminopropyl chloride hydrochloride in place of 2-diethylaminoethyl chloride hydrochloride, and using 5-chloroisatin in place of the compound of reference example 1.

Workup

  1. customThis compound was prepared by the same method as

Sources & evidence

ORD record
ord-18cc24d2796e48c2ae3952f21ffbf00f
Source dataset
uspto-grants-2003_06
Patent number
US06576656B1

Reaction notes

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