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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351702Generated: October 29, 2026

N-butyl-4-(4-oxo-piperidin-1-yl)-benzenesulfonamide → N-Butyl-4-{4-[(2S)-3-(9H-carbazol-4-yloxy)-2-hydroxy-propylamino]-piperidin-1-yl}-benzenesulfonamide

https://huagongshe.com/reaction/351702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-butyl-4-(4-oxo-piperidin-1-yl)-benzenesulfonamideHCID 12051795—
Reactant1-Amino-3-(9H-carbazol-4-yloxy)-2-propanolHCID 14893806—
ProductN-Butyl-4-{4-[(2S)-3-(9H-carbazol-4-yloxy)-2-hydroxy-propylamino]-piperidin-1-yl}-benzenesulfonamideHCID 10166150—

Reaction Steps

The title compound was prepared from 1-amino-3-(9H-carbazol-4-yloxy)-propan-2-ol and Reference Example 11, N-butyl-4-(4-oxo-piperidin-1-yl)-benzenesulfonamide, according to the procedure of Example 1 as an off-white solid; mp 166-179° C.; 1H NMR (300 MHz, DMSO-d6) δ 0.79 (t, 3H), 1.15-1.40 (m, 6H), 1.75-1.90 (m, 2H), 2.64 (t, 2H), 2.60-3.00 (m, 5H), 3.60-4.20 (m, 5H), 6.69 (d, 1H), 6.80-7.60 (m, 7H), 7.90 (s, 1H), 8.20 (d, 2H), 11.35 (s, 1H); MS (ES) m/z: 551.1 (MH+); HRMS Calcd. for C30H39N4O4S (MH+): 551.2692. Found: 551.2664.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743787B2
Source datasetuspto-grants-2004_06
ORD IDord-f2fe79e001f0446da81878fa78e2a8df
Source noteuspto-grants-2004_06