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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192495Generated: November 1, 2026

Ammonium Acetate → 1-{5-Chloro-8-[4-(2-methoxyethyl)piperazin-1-yl]quinolin-7-yl]ethanamine

https://huagongshe.com/reaction/1192495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-{5-Chloro-8-[4-(2-methoxyethyl)piperazin-1-yl]quinolin-7-yl}ethanoneHCID 67301675—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
Product1-{5-Chloro-8-[4-(2-methoxyethyl)piperazin-1-yl]quinolin-7-yl]ethanamineHCID 67301134—

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 1-{5-chloro-8-[4-(2-methoxyethyl)piperazin-1-yl]quinolin-7-yl}ethanone (22 mg, 0.063 mmol) and ammonium acetate (48.8 mg, 0.632 mmol) in methanol (0.36 mL) and acetonitrile (0.36 mL) was heated at 65° C. in a sealed tube for 30 minutes. After cooling, sodium cyanoborohydride (7.95 mg, 0.126 mmol) was added to the resultant mixture. The reaction was heated at 65° C. for another 4 hours, then cooled to room temperature, quenched with saturated sodium bicarbonate, and extracted with dichloromethane. The combined extracts were dried over magnesium sulfate and evaporated to dryness (22 mg, 99%). The residue was used directly in the next step. LCMS calculated for C18H26ClN4O(M+H)+: m/z=349.2; found: 349.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680108B2
Source datasetuspto-grants-2014_03
ORD IDord-b8d304d8a95b412fb2aaf57d8fc28dc7
Source noteuspto-grants-2014_03