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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595946Generated: October 30, 2026

HCID 118045361, compound → HCID 118045348, compound

https://huagongshe.com/reaction/595946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 118045361HCID 118045361—
SolventEthanolHCID 702—
ProductHCID 118045348HCID 118045348—

Reaction Steps

(+/−)-4-(2-amino-5-bromopyridin-3-yl)-2-fluoro-N-((1S,2R)-2-phenylcyclopropyl)benzamide (121 mg) was resolved by chrial chromatography (AD-H column EtOH=60/40, 1 mL/min). The polar compound (Peak1), 4-(2-amino-5-bromopyridin-3-yl)-2-fluoro-N-((1R,2S)-2-phenylcyclopropyl)benzamide, was obtained at 7.41 min (50 mg, 41%) and the less polar compound (Peak2), 4-(2-amino-5-bromopyridin-3-yl)-2-fluoro-N-((1S,2R)-2-phenylcyclopropyl)benzamide, was obtained at 10.26 min (54 mg, 44%). The absolute stereochemistry was assigned based on biochemical data and docking model of the corresponding analogs.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-9f279575a6f9432d85695e6af0283182
Source noteuspto-grants-2016_01