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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198499Generated: October 26, 2026

Ethyl 2-bromopropionate → ethyl 2-{4-[N-methyl-N-(6,7-dichloro-2-quinoxalinyl)amino]phenoxy}propionate

https://huagongshe.com/reaction/2198499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-bromopropionateHCID 79040—
Reactant4-[N-methyl-N-(6,7-dichloro-2-quinoxalinyl)amino]phenolHCID 13323142—
Productethyl 2-{4-[N-methyl-N-(6,7-dichloro-2-quinoxalinyl)amino]phenoxy}propionateHCID 13323143—

Reaction Steps

4-[N-Methyl-N-(6,7-dichloro-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-(6,7-dichloro-2-quinoxalinyl)amino]phenoxy}propionate, mp 79° C. Proton magnetic resonance spectrum (CDCl3 ; δ in ppm): 8.25 (1H, s, quinoxaline hetero-ring proton); 7.9 (1H, s, quinoxaline benzo-ring proton); 7.8 (1H, s, quinoxaline benzo-ring proton); 7.2 (4H, m, phenoxy protons); 4.85 (1H, q, CH-CH3); 4.3 (2H, q, CH2 -CH3); 3.55 (3H, s, N-CH3); 1.7 (3H, d, CH-CH3); 1.3 (3H, t, CH2 -CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04358307
Source datasetuspto-grants-1982_11
ORD IDord-bb5f2f760e524e0c99976d1d839d2a4b
Source noteuspto-grants-1982_11