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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237260Generated: October 31, 2026

2-Chloro-4-pyridinecarboxaldehyde → HCID 59853074, compound

https://huagongshe.com/reaction/2237260

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4-pyridinecarboxaldehydeHCID 2762994—
ReactantN-Boc-4-broMo-3-fluoroanilineHCID 59852943—
ReactantHCID 178418306HCID 178418306—
ReactantHCID 178418689HCID 178418689—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59853074HCID 5985307441%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of tert-butyl 4-bromo-3-fluorophenylcarbamate (2.60 g, 9.0 mmol) in anhydrous THF (30 mL) at −78° C. was added MeMgBr (3.0 M in Et2O, 3.1 mL, 9.3 mmol) via syringe. The solution was stirred for 10 min at that temperature, and then warmed to 0° C. for 0.5 h. After the solution was cooled back to −78° C., a solution of t-BuLi (1.7 M in hexane, 10.6 mL, 18.1 mmol) was added over 4 min. The resulting solution was allowed to stir for 5 min before a solution of 2-chloroisonicotinaldehyde (1.41 g, 10 mmol) (for preparation, see Frey, L. F. et al. Tetrahedron Lett. 2001, 42, 6815) in anhydrous THF (25 mL) was added in 3 min. The reaction mixture was stirred at −78° C. for 20 min and 2.0 mL of MeOH was added. The solution was then concentrated under reduced pressure and the residue was dissolved in 200 mL of EtOAc. It was subsequently washed with H2O (2×50 mL), brine (2×50 mL) and dried over MgSO4. After filtration and concentration, the residue was purified by flash chromatography on SiO2 eluting with 0%-50% EtOAc in hexane to give tert-butyl 4-((2-chloropyridin-4-yl)(hydroxy)methyl)-3-fluorophenylcarbamate (1.30 g, 41% yield). MS(ESI+): m/z 353.28/355.24 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714138B2
Source datasetuspto-grants-2010_05
ORD IDord-3c899ab97e1d42e987be763bd64df759
Source noteuspto-grants-2010_05