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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50820Generated: October 28, 2026

3-Bromoaniline → N-(3-bromophenyl)pyrido[3,4-d]pyrimidin-4-amine

https://huagongshe.com/reaction/50820

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromoanilineHCID 11562—
Reactant4-Methylthiopyrido[3,4-d]pyrimidineHCID 23240465—
ProductN-(3-bromophenyl)pyrido[3,4-d]pyrimidin-4-amineHCID 532825752.7%

Reaction Conditions

Temperature10 °C

Reaction Steps

A mixture of 4-methylthiopyrido[3,4-d]pyrimidine (75 mg, 0.42 mmol) (see previous experimental), and 3-bromoaniline (1 mL) is heated to 10° C. under N2 for 2 h. The reaction mixture is then chromatographed on silica using MPLC and eluting with a gradient system (CHCl3 to 5% MeOH in CHCl3). The fractions are concentrated under reduced pressure, and the resulting solid is recrystallized from Et2O to yield 4-(3-bromoanilino)pyrido[3,4-d]pyrimidine (66 mg, 52.7%) as a light brown solid. 1H NMR (DMSO) δ 10.15 (1H, s), 9.21 (1H, s), 8.80 (1H, s), 8.76 (1H, d, J=5.8 Hz), 8.44 (1H, d, J=5.6 Hz), 8.25 (1H, s), 7.93 (1H, d, J=7.7 Hz), 7.45-7.37 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713484B2
Source datasetuspto-grants-2004_03
ORD IDord-e47552f259f0432bba4aee43fc64e471
Source noteuspto-grants-2004_03