Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839049Generated: October 30, 2026

4-Fluorobenzenesulfonyl chloride → HCID 11605326, compound

https://huagongshe.com/reaction/1839049

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
ReactantHCID 22344444HCID 22344444—
ProductHCID 11605326HCID 11605326—

Reaction Steps

According to the general method of Example 5, 1-(4-aminobutyl)-2-(2-methoxyethyl)-6,7,8,9-tetrahydro-1H-imidazo[4,5-c]quinolin-4-amine and 4-fluorobenzenesulfonyl chloride were combined. Recrystallization from 4:1 n-propyl acetate\methanol provided N1-{4-[4-amino-2-(2-methoxyethyl)-6,7,8,9-tetrahydro-1H-imidazo[4,5-c]quinolin-1-yl]butyl}-4-fluoro-1-benzenesulfonamide as a white crystalline solid, m.p. 191.0-193.0° C. 1H NMR (300 MHz, DMSO-d6) δ 7.86-7.81 (m, 2H), 7.67 (broad s, 1H), 7.45-7.39 (m, 2H), 5.65 (broad s, 2H), 4.15 (m, 2H), 3.76 (t, J=6.7 Hz, 2H), 3.27 (s, 3H), 3.00 (t, J=6.7 Hz, 2H), 2.90 (broad s, 2H), 2.78 (m, 2H), 2.65 (broad s, 2H), 1.75 (broad s, 4H), 1.61 (m, 2H), 1.43 (m, 2H); MS (CI) m/e 476 (M+H). Analysis: Calculated for C23H30FN5O3S: %C, 58.09; %H, 6.36; %N, 14.73; Found: %C, 58.37; %H, 6.35; %N, 14.60.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677349B1
Source datasetuspto-grants-2004_01
ORD IDord-dacf28794f6f4f86b0e8b77bebc43117
Source noteuspto-grants-2004_01