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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281949Generated: October 30, 2026

N-(3-bromophenyl)-7-fluoropyrido[4,3-d]pyrimidin-4-amine → N-(3-bromophenyl)-7-methoxypyrido[4,3-d]pyrimidin-4-amine

https://huagongshe.com/reaction/1281949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-bromophenyl)-7-fluoropyrido[4,3-d]pyrimidin-4-amineHCID 5328251—
ReactantSodium methanolate methanolHCID 23694274—
ProductN-(3-bromophenyl)-7-methoxypyrido[4,3-d]pyrimidin-4-amineHCID 532825489%

Reaction Steps

A solution of 7-fluoro-4-(3-bromoanilino)pyrido[4,3-d]pyrimidine (100 mg, 0.31 mmol) in 1 M sodium methoxide-methanol (30 mL) is stirred under reflux for 42 h. The resulting mixture is concentrated under reduced pressure, diluted with water and neutralized with dilute HCl to give 7-methoxy-4-(3-bromoanilino)pyrido[4,3-d]pyrimidine (92 mg, 89%) as a white solid. 1H NMR (DMSO) δ 10.22 (1H, brs), 9.57 (1H, s), 8.63 (1H, s), 8.19 (1H, s), 7.86 (1H, brd, J=7.9 Hz), 7.39 (1H, t, J=7.9 Hz), 7.35 (1H, dd, J=7.9, 1.5 Hz), 6.96 (1H, s), 4.00 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455534B2
Source datasetuspto-grants-2002_09
ORD IDord-0546fbee67be40f8a41936f4d6c6521a
Source noteuspto-grants-2002_09