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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274893Generated: November 1, 2026

2-Bromo-5-fluoropyridine → HCID 90386053, compound

https://huagongshe.com/reaction/2274893

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-5-fluoropyridineHCID 2783171—
ReactantHCID 131733412HCID 131733412—
ProductHCID 90386053HCID 9038605334%

Reaction Steps

Using general procedure E, (S)-quinuclidin-3-yl(1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxa-borolan-2-yl)phenyl)cyclopropyl)carbamate, 2-bromo-5-fluoropyridine and [PdCl2(pddf)]CH2Cl2 gave the title compound as a white solid (34%). 1H NMR (500 MHz, CDCl3) δ 8.51-8.52 (d, J=3.5 Hz, 1H), 7.87-7.85 (d, J=10.5 Hz, 2H), 7.69-7.67 (m, 1H), 7.47-7.42 (m, 1H), 7.32-7.27 (m, 2H), 5.79-5.66 (d, 1H), 4.73-4.71 (t, J=5.0 Hz, 1H), 3.22-3.19 (m, 1H), 2.87-2.61 (m, 5H), 2.01-1.22 (m, 9H) ppm. 13C NMR (125 MHz, CDCl3) δ 160.8, 157.4, 156.1, 153.5, 144.4, 137.8, 136.3, 126.7, 125.7, 124.9, 123.6, 121.1, 71.6, 55.7, 47.4, 46.5, 35.3, 29.7, 25.4, 24.8, 19.4, 18.2 ppm. Purity: >99% LCMS (214 nm & 254 nm); retention time 1.41 min; (M+1) 382.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126993B2
Source datasetuspto-grants-2015_09
ORD IDord-7e4f504172f74c8ea1357be760c11f6d
Source noteuspto-grants-2015_09