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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355468Generated: November 1, 2026

Acetic Acid → 1-[4-(2-Chloro-3-fluoro-pyridin-4-ylmethyl)-piperazin-1-yl]-ethanone

https://huagongshe.com/reaction/1355468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1-AcetylpiperazineHCID 83795—
Reactant2-Chloro-3-fluoro-4-formylpyridineHCID 2763160—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
Product1-[4-(2-Chloro-3-fluoro-pyridin-4-ylmethyl)-piperazin-1-yl]-ethanoneHCID 18506923—

Reaction Steps

1-Acetylpiperazine (0.164 g 1.28 mmol)was dissolved in 5 mL DCE and the resulting solution was added to 2-chloro-3-fluoro-pyridine-4-carbaldehyde (14-2, 0.170 g, 1.07 mmol). NaBH(OAc)3 (0.248 g, 1.17 mmol) was added followed by the addition of 0.100 mL of HOAc. After 45 min the reaction was quenched with sat NaHCOC3 (aq). The mixture was extracted 3× with DCM, and the organic extracts were dried over Na2SO4, filtered and concentrated. The residue was purified by flash column chromatography (10 g column, DCM (for 4 min) gradient to 95:5 DCM/MeOH (over 8 min)), desired comes off shortly after 95:5 is attained (13 min) affording good separation from close peak preceeding desired. Afforded pure titled compound. 1H NMR (CDCl3) δ8.18 (d, 1H, J=4.9 Hz), 7.38 (t, 1H, J=4.6 Hz), 3.66 (m, 4H), 3.50 -3.48 (m, 2H), 2.50-2.46 (m, 4H), 2.09 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586423B2
Source datasetuspto-grants-2003_07
ORD IDord-0cce764e5760463ca9dac95a1a38372f
Source noteuspto-grants-2003_07