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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074608Generated: October 25, 2026

2-(Bromomethyl)-4-chloro-1-(trifluoromethyl)benzene → HCID 57886085, compound

https://huagongshe.com/reaction/2074608

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Bromomethyl)-4-chloro-1-(trifluoromethyl)benzeneHCID 2778116—
Reactant7-iodo-3,4-dihydropyrido[2,3-b]pyrazin-2(1H)-oneHCID 44829114—
ReactantHCID 57886049HCID 57886049—
ProductHCID 57886085HCID 5788608517%

Reaction Steps

7-Iodo-3,4-dihydro-1H-pyrido[2,3-b]pyrazin-2-one (968 mg) was reacted with 5-chloro-2-(trifluoromethyl)benzyl bromide as in General Procedure 1. The resulting 1-(2-chloro-5-trifluoromethylbenzyl)-7-iodo-3,4-dihydro-1H-pyrido[2,3-b]pyrazin-2-one was reduced as in General Procedure 2 to give the title compound as an orange solid (17% yield). M.p. 189-191° C., LCMS: m/z=454.08 (M+H+), 1H-NMR (DMSO-d6, 400 MHz) δ 3.28-3.34 (m, 2H), 3.41-3.46 (m, 2H), 4.53 (s, 2H), 6.52 (s, 1H), 6.75 (s, 1H), 7.44 (s, 2H), 7.59 (d, J=8.4 Hz, 1H), 7.82 (d, J=8.6 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919502B2
Source datasetuspto-grants-2011_04
ORD IDord-cf2894e8f8784d75a5d9a3eb13b48c66
Source noteuspto-grants-2011_04