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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274877Generated: October 31, 2026

(Pyrimidin-5-yl)boronic acid → HCID 123591011, compound

https://huagongshe.com/reaction/2274877

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Pyrimidin-5-yl)boronic acidHCID 2795193—
ReactantHCID 123505138HCID 123505138—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 123591011HCID 12359101132.8%

Reaction Steps

Using general procedure E, 1-azabicyclo[2.2.2]oct-3-yl[2-(3-bromo-4-fluorophenyl)propan-2-yl]carbamate (150 mg, 0.389 mmol), pyrimidine-5-boronic acid (75.9 mg, 0.613 mmol) and tris(dibenzylideneacetone)dipalladium(0) gave the title compound as a white solid (49 mg, 31%). 1H NMR (400 MHz, CDCl3) δ 9.22 (s, 1H), 8.92 (s, 2H), 7.55-7.41 (m, 2H), 7.19 (dd, J=8.7, 9.9 Hz, 1H), 5.37 (s, 1H), 4.72-4.49 (m, 1H), 3.34-2.04 (m, 6H), 2.04-0.98 (m, 5H), 1.66 (t, J=10.9 Hz, 6H) ppm. 13C NMR (100 MHz, CDCl3) δ 159.9, 157.9, 157.4, 156.6, 154.7, 130.2, 127.85, 127.77, 126.9, 122.0, 121.8, 116.7, 116.5, 116.2, 71.6, 55.9, 54.9, 47.6, 46.7, 30.3, 29.6, 25.6, 24.8, 19.8 ppm. Purity: 93% UPLCMS (210 nm); retention time 0.63 min; (M+1) 384.9

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126993B2
Source datasetuspto-grants-2015_09
ORD IDord-359a2e62ed3245feb11714e813a7a7ac
Source noteuspto-grants-2015_09