2-Chloroethyldiisopropylammonium chloride → HCID 21287236, compound

HRID 868565Notes

Reaction equation

HRID 868565 reaction equation
[NH:1]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][C:10]=2[C:12]([O:14][CH3:15])=[O:13])[C:4](=[O:5])[C:2]1=[O:3].Cl.[CH:17]([N:20]([CH:24]([CH3:26])[CH3:25])[CH2:21][CH2:22]Cl)([CH3:19])[CH3:18]>>[CH:17]([N:20]([CH:24]([CH3:26])[CH3:25])[CH2:21][CH2:22][N:1]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][C:10]=2[C:12]([O:14][CH3:15])=[O:13])[C:4](=[O:5])[C:2]1=[O:3])([CH3:19])[CH3:18]

Participants

3

Reactant 2

HCID 779422-Chloroethyldiisopropylammonium chlorideHCID 1946733Methyl 2,3-dioxo-2,3-dihydro-1H-indole-7-carboxylate

Product 1

HCID 21287236HCID 21287236, compound

Procedure

By using methyl 7-isatincarboxylate and 2-diisopropylaminoethyl chloride hydrochloride, a method analogous to that described in Reference Example 7 was carried out to obtain methyl 1-(2-diisopropylaminoethyl)-7-isatincarboxylate in an oil (yield: 94.6%).

Sources & evidence

ORD record
ord-c58090f7ed954c9cad475ef0f5419782
Source dataset
uspto-grants-1988_10
Patent number
US04780477

Reaction notes

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