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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871935Generated: October 30, 2026

5-Amino-2-fluoropyridine → HCID 57986920, compound

https://huagongshe.com/reaction/871935

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Amino-2-fluoropyridineHCID 819440—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl 4-(4-formyl-1,3-thiazol-2-yl)piperidine-1-carboxylateHCID 7172298—
SolventDichloromethaneHCID 6344—
ProductHCID 57986920HCID 57986920—

Reaction Steps

5-amino-2-fluoropyridine (0.476 g, 4.2 mmol) was added to 4-(4-Formyl-thiazol-2-yl)-piperidine-1-carboxylic acid tert-butyl ester (0.84 g, 2.8 mmol) in dry DCM (10 mL). Sodium triacetoxyborohydride (0.9 g, 4.2 mmol) was then added. The reaction was stirred for 3 hours at room temperature under N2. The organic layer was washed with 2M NaOH solution, water, brine, dried (MgSO4), and the solvent was removed in vacuo. The material was purified by silica gel chromatography (DCM/methanol: 10:1 v/v) to give the desired product. 1H NMR (CDCl3): δ 7.59-7.60 (1H, m), 7.06-7.10 (1H, m), 7.02 (1H, s), 6.76 (1H, dd, J=8.8, 3.6 Hz), 4.4 (2H, d), 4.20-4.31 (3H, m), 3.09-3.17 (1H, m), 2.8-2.95 (2H, m), 2.07-2.10 (2H, m), 1.77-1.47, (2H, m), 1.47 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975258B2
Source datasetuspto-grants-2015_03
ORD IDord-2854b585bc47417fa365f0549181a7c8
Source noteuspto-grants-2015_03