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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171392Generated: October 26, 2026

1-Acetylpiperazine → n-{4-[3-(4-Acetyl-piperazin-1-yl)-propoxy]-naphthalen-1-yl}-3-fluoro-5-piperidin-1-yl-benzamide

https://huagongshe.com/reaction/1171392

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-AcetylpiperazineHCID 83795—
ReactantN-[4-(3-chloropropoxy)-naphthalen-1-yl]-3-fluoro-5-piperidin-1-yl-benzamideHCID 59553319—
Productn-{4-[3-(4-Acetyl-piperazin-1-yl)-propoxy]-naphthalen-1-yl}-3-fluoro-5-piperidin-1-yl-benzamideHCID 59553105—

Reaction Steps

Compound is prepared from N-[4-(3-chloropropoxy)-naphthalen-1-yl]-3-fluoro-5-piperidin-1-yl-benzamide and N-acetylpiperizine according to conditions described in general procedure L. A white powder (0.13 g, 75.5%). Mp: 210-211° C. 1H NMR (300 MHz, DMSO-d6) δ 10.23 (s, 1H), 8.22 (br s, 1H), 7.84 (br s, 1H), 7.55 (m, 2H), 7.44 (m, 2H), 7.15 (br s, 1H), 6.98 (br s, 2H), 4.23 (br s, 2H), 3.42 (br s, 4H), 3.30 (br s, 4H), 2.57 (br s, 2H), 2.42 (m, 4H), 2.04 (m, 2H), 1.98 (s, 3H), 1.60 (br s, 6H). MS: 533.5 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829560B2
Source datasetuspto-grants-2010_11
ORD IDord-8fa8514a06e6494a9912660871a214dd
Source noteuspto-grants-2010_11