Ethyl 2-bromopropionate → HCID 20519108, compound

HRID 2198501Notes

Reaction equation

HRID 2198501 reaction equation
[CH3:1][N:2]([C:14]1[CH:19]=[CH:18][C:17]([OH:20])=[CH:16][CH:15]=1)[C:3]1[C:12]([Cl:13])=[N:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[N:4]=1.Br[CH:22]([CH3:28])[C:23]([O:25][CH2:26][CH3:27])=[O:24]>>[CH3:1][N:2]([C:14]1[CH:19]=[CH:18][C:17]([O:20][CH:22]([CH3:28])[C:23]([O:25][CH2:26][CH3:27])=[O:24])=[CH:16][CH:15]=1)[C:3]1[C:12]([Cl:13])=[N:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[N:4]=1

Participants

3

Reactant 2

HCID 79040Ethyl 2-bromopropionateHCID 20519119HCID 20519119, compound

Product 1

HCID 20519108HCID 20519108, compound

Procedure

4-[N-Methyl-N-(3-chloro-2-quinoxalinyl)amino]phenol was reacted with ethyl 2-bromopropionate, following essentially the same procedure as that described in Example 1 Part (b), to give ethyl 2-{4-[N-methyl-N-(3-chloro-2-quinoxalinyl)amino]phenoxy}propionate as an oil.

Sources & evidence

ORD record
ord-fce49ac3ffdc4df38e3c34ae27fe92f8
Source dataset
uspto-grants-1982_11
Patent number
US04358307

Reaction notes

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