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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710001Generated: October 29, 2026

Hydrogen Bromide → HCID 86267825, compound

https://huagongshe.com/reaction/710001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantHCID 90417260HCID 90417260—
SolventAcetic AcidHCID 176—
ProductHCID 86267825HCID 8626782559.6%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 4-methoxy-5-(4-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)-2-(pyrrolidin-1-yl)pyrimidine (0.19 g, 0.43 mmol) in acetic acid (2.5 mL) was treated with HBr (48%, 0.10 mL, 1.8 mmol) and heated at 90° C. for 16 h. The mixture was poured onto ice (10 g), neutralized with satd. NaHCO3, and the resulting solid was collected by filtration, washed with water and MeCN and dried to afford 5-(4-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)-2-(pyrrolidin-1-yl)pyrimidin-4(3H)-one (0.11 g, 58%). 1H NMR (400 MHz, DMSO-d6): δ 11.22 (bs, 1H), 8.68 (s, 1H), 8.38 (s, 1H), 8.34 (d, J=5.7 Hz, 1H), 8.30 (d, J=1.3 Hz, 1H), 8.26 (s, 1H), 7.96 (s, 1H), 7.22 (d, J=2.4 Hz, 1H), 6.60-6.58 (m, 1H), 3.84 (s, 3H), 3.50 (bs, 4H), 2.15 (s, 3H), 1.91 (bs, 4H); MS (ESI) m/z: 430.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181223B2
Source datasetuspto-grants-2015_11
ORD IDord-3140457d48074d39a4a286686bbf1b35
Source noteuspto-grants-2015_11