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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274887Generated: October 31, 2026

Phenylboronic Acid → HCID 68327850, compound

https://huagongshe.com/reaction/2274887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
ReactantHCID 68327753HCID 68327753—
Catalystpalladium(II) acetateHCID 167845—
ProductHCID 68327850HCID 6832785066.3%

Reaction Steps

Using general procedure E, N-[2-(3-bromo-4-fluorophenyl)propan-2-yl]-1,4-diazabicyclo[3.2.2]nonane-4-carboxamide (100 mg, 0.261 mmol), phenylboronic acid (79 mg, 0.65 mmol) and palladium (II) acetate gave the title compound as an off-white solid (66 mg, 66%). 1H NMR (400 MHz, CDCl3) δ 7.54 (m, 2H), 7.44-7.40 (m, 5H), 7.08(m, 1H), 4.78(br s, 1H), 4.00 (br s, 1H), 3.60 (m, 2H), 3.11-2.92 (m, 6H), 2.00 (m, 2H) 1.67(m, 7H), 1.26 (s, 1H) ppm. 13C NMR (100 MHz, CDCl3) δ 159.6, 155.6, 144.6, 136.5, 129.3, 128.6, 128.5, 127.8, 127.5, 125.7, 125.6, 116.1, 115.9, 57.9, 55.3, 48.2, 46.4, 46.4, 41.6, 30.6, 30.5, 29.9, 27.6 ppm. Purity: >99% UPLCMS (210 nm); retention time 0.88 min; (M+1) 382.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126993B2
Source datasetuspto-grants-2015_09
ORD IDord-35676b59605840e48e5b320041a488fa
Source noteuspto-grants-2015_09