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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171363Generated: October 26, 2026

3-Furanmethanol → 3-Fluoro-N-[4-(3-furylmethoxy)-1-naphthyl]-5-piperidin-1-ylbenzamide

https://huagongshe.com/reaction/1171363

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-FuranmethanolHCID 20449—
Reactanttert-Butyl (4-hydroxynaphthalen-1-yl)carbamateHCID 10923237—
Reactant3-Fluoro-5-piperidinylbenzoic acidHCID 59553180—
Product3-Fluoro-N-[4-(3-furylmethoxy)-1-naphthyl]-5-piperidin-1-ylbenzamideHCID 59553349—

Reaction Steps

Compound is prepared from tert-butyl (4-hydroxy-1-naphthyl)carbamate, 3-fluoro-5-piperidin-1-yl-benzoic acid and furan-3-yl-methanol according to conditions described in general procedure D. A pink solid is produced (12 mg). Mp: 152-153° C.; 1H NMR (300 MHz, CDCl3) δ 1.63-1.69 (m, 6H), 3.20-3.27 (m, 2H), 5.13 (s, 2H), 6.58 (s, 1H), 6.75 (d, J=12.6 Hz, 1H), 6.89 (d, J=8.4 Hz, 1H), 6.98 (d, J=9.0 Hz, 1H), 7.30 (s, 1H), 7.47-7.59 (m, 4H), 7.12 (d, J=8.1Hz, 1H), 7.83 (d, J=8.4 Hz, 1H), 7.95 (s, 1H), 8.32 (d, J=8.1Hz, 1H); MS 445 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829560B2
Source datasetuspto-grants-2010_11
ORD IDord-32e0ed3acc01423193cb70f7569e1104
Source noteuspto-grants-2010_11