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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353880Generated: October 25, 2026

Quinaldoyl chloride → HCID 23512713, compound

https://huagongshe.com/reaction/353880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinaldoyl chlorideHCID 2760547—
Reactant1-(4-aminobutyl)-2-phenyl-1H-imidazo[4,5-c]quinolin-4-amineHCID 12148992—
ProductHCID 23512713HCID 23512713—

Reaction Steps

According to the general method of Example 61, 1-(4-aminobutyl)-2-phenyl-1H-imidazo[4,5-c]quinolin-4-amine and quinoline-2-carbonyl chloride were combined to provide N2-[4-(4-amino-2-phenyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-2-quinolinecarboxamide as an off white crystalline solid, m.p. 81.1-83.9° C. 1H NMR (300 MHz, DMSO-d6) δ 8.90 (t, J=6.0 Hz, 1H), 8.55 (d, J=8.5 Hz, 1H), 8.12-8.07 (m, 4H), 7.90-7.84 (m, 1H), 7.75-7.54 (m, 7H), 7.36 (t, J=7.5 Hz, 1H), 7.18 (t, J=7.5 Hz, 1H), 6.70 (broad s, 2H), 4.61 (m, 2H), 3.23 (m, 2H), 1.88 (m, 2H), 1.49 (m, 2H); MS (CI) m/e 487 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756382B2
Source datasetuspto-grants-2004_06
ORD IDord-7c5d33eb1c8c490aab07992513f41cb1
Source noteuspto-grants-2004_06