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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1-Acetylpiperazine | HCID 83795 | — |
| Reactant | 2-Chloro-3-fluoro-4-formylpyridine | HCID 2763160 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 1-[4-(2-Chloro-3-fluoro-pyridin-4-ylmethyl)-piperazin-1-yl]-ethanone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06586423B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-0cce764e5760463ca9dac95a1a38372f |
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| Source note | uspto-grants-2003_07 |
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