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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930828Generated: October 30, 2026

Bromide ion → HCID 86281290, compound

https://huagongshe.com/reaction/930828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
Reactant4-(Methoxycarbonylamino)phenylboronic acidHCID 2773494—
ReactantHCID 90412061HCID 90412061—
SolventMethanolHCID 887—
ProductHCID 86281290HCID 86281290—

Reaction Steps

Compound 24 was synthesized using N-(3-(6-bromoimidazo[1,2-a]pyrimidin-2-yl)-4-chlorophenyl)pyrrolidine-1-carboxamide (I-15) as the bromide and (4-((methoxycarbonyl)amino)phenyl)boronic acid using a suzuki coupling protocol as described in the synthesis of I-11. The residue was redissolved in methanol and precipitation yielded the compound. m/z (ESI) of 24: 491.2 (M+H+), 1H NMR (600 MHz, DMSO-D6) δ 9.86 (s, 1H), 9.30 (d, J=2.6, 1H), 8.94 (d, J=2.6, 1H), 8.55 (s, 1H), 8.47 (d, J=2.8, 2H), 7.73 (m, 3H), 7.62 (d, J=8.5, 2H), 7.41 (d, J=8.8, 1H), 3.70 (s, 3H), 3.40 (t, J=6.5, 4H), 1.86 (t, J=6.4, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296754B2
Source datasetuspto-grants-2016_03
ORD IDord-e2b78c93d71d49309b6bd76f6ef91a7f
Source noteuspto-grants-2016_03