Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353867Generated: October 30, 2026

6-Chloronicotinoyl Chloride → HCID 23512687, compound

https://huagongshe.com/reaction/353867

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloronicotinoyl ChlorideHCID 2782165—
Reactant1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 15453775—
ProductHCID 23512687HCID 23512687—

Reaction Steps

According to the general method of Example 14, 1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amine and 6-chloropyridine-3-carbonyl chloride were combined to provide N3-[4-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-6-chloronicotinamide as an off white crystalline solid, m.p. 144.0-148.0° C. (decomposition). 1H NMR (300 MHz, DMSO-d6) δ 8.77 (dd, J=2.5, 0.6 Hz, 1H), 8.73 (t, J=5.6 Hz, 1H), 8.22 (s, 1H), 8.16 (dd, J=8.3, 2.5 Hz, 1H), 8.03 (m, 1H), 7.63 (d, J=0.5 Hz, 1H), 7.60 (d, J=0.5 Hz, 1H), 7.45-7.40 (m, 1H), 7.23-7.18 (m, 1H), 6.61 (broad s, 2H), 4.63 (t, J=6.9 Hz, 2H), 3.30 (m,2H), 1.92 (m, 2H), 1.58 (m, 2H). MS (EI) m/e 394.1298 (394.1309 calcd for C20H19N6OCl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756382B2
Source datasetuspto-grants-2004_06
ORD IDord-af123e8c7b19423d847210584a7dc98c
Source noteuspto-grants-2004_06