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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102821Generated: October 29, 2026

Hydrochloric Acid → N-(6-{7-Methoxy-6-[3-(4-methylpiperazin-1-yl)propoxy]quinazolin-4-ylamino}-benzothiazol-2-yl)benzamide

https://huagongshe.com/reaction/2102821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(6-amino-1,3-benzothiazol-2-yl)benzamideHCID 810331—
Reactant4-Chloro-7-methoxy-6-(3-(4-methylpiperazin-1-yl)propoxy)quinazolineHCID 23132474—
Solvent1-ButanolHCID 263—
ProductN-(6-{7-Methoxy-6-[3-(4-methylpiperazin-1-yl)propoxy]quinazolin-4-ylamino}-benzothiazol-2-yl)benzamideHCID 44467679—

Reaction Steps

N-(6-{7-Methoxy-6-[3-(4-methylpiperazin-1-yl)propoxy]quinazolin-4yl-amino}benzothiazol-2-yl)benzamide was prepared by heating a mixture of N-(6-amino-benzothiazol-2-yl)benzamide (Intermediate 2, 40 mg. 0.148 μmol), 4-chloro-7-methoxy-6-[3-(4methylpiperazin-1-yl)propoxy]quinazoline (IM 8, 52 mg, 0.148 mmol), and HCl (112 μL, 4 M solution in dioxane, 0.444 mmol) in n-butanol (6 mL) to 110° C. for 5 h. Saturated sodium hydrogencarbonate solution was added and the product was extracted with ethyl acetate. After washing with water and drying over Na2SO4, the solvent was removed. The residue was taken up in little methanol, then water was slowly added. After stirring the mixture overnight, a grey solid was obtained (39 mg, 66 μmol, 45%). LC(ESI-MS: m/z=584 [M+H]+; m/z=582 [M−H]−; Rt=2.26 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576090B2
Source datasetuspto-grants-2009_08
ORD IDord-03b25521725f4b7bb467a31942416312
Source noteuspto-grants-2009_08