Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50767Generated: October 25, 2026

Water → N-(3-bromophenyl)-6-fluoropyrido[3,2-d]pyrimidin-4-amine

https://huagongshe.com/reaction/50767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-BromoanilineHCID 11562—
Reactant4-Chloro-6-fluoropyrido[3,2-D]pyrimidineHCID 10631322—
CatalystHydrochloric AcidHCID 313—
SolventIsopropanolHCID 3776—
ProductN-(3-bromophenyl)-6-fluoropyrido[3,2-d]pyrimidin-4-amineHCID 5328276—

Reaction Steps

A solution of 4-chloro-6-fluoropyrido[3,2-d]pyrimidine (0.20 g, 1.1 mmol) and 3-bromoaniline (0.12 mL, 2.18 mmol) in propan-2-ol(20 mL) containing conc. HCl (1 drop) is heated under reflux for 15 min, then cooled, poured into water and extracted with EtOAc. The extract is worked up, and the residue chromatographed on silica gel, eluting with EtOAc/petroleum ether (1:2)to give after removal of the solvent under reduced pressure 4-(3-bromoanilino)-6-fluoropyrido[3,2-d]pyrimidine (0.18 g, 52%). 1H NMR (CDCl3) δ 8.82 (1H, s), 8.65 (1H, brs), 8.31 (1H, t, J=7.4 Hz), 8.27 (1H, brs), 7.77 (1H, m) 7.41 (1H, dd, J=8.9, 2.2 Hz), 7.29 (2H, brs).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713484B2
Source datasetuspto-grants-2004_03
ORD IDord-5c042fc5759c4b4bb29e118df015b6b0
Source noteuspto-grants-2004_03