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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408363Generated: November 3, 2026

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

https://huagongshe.com/reaction/1408363

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 numberUS08921350B2
Source datasetuspto-grants-2014_12
ORD IDord-a46e7fbb50864bdba5a36c909a5c3658
Source noteuspto-grants-2014_12