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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736757Generated: October 29, 2026

Acetyl chloride → HCID 68817368, compound

https://huagongshe.com/reaction/736757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantHCID 68819516HCID 68819516—
SolventDichloromethaneHCID 6344—
ProductHCID 68817368HCID 6881736892.1%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 4-[4-(2-methyl-quinolin-4-ylmethoxy)-benzenesulfonylamino]-piperidine-3-carboxylic acid ethyl ester (0.6 g, 1.24 mmol) in CH2Cl2 (10 mL) and TEA (0.378 mL, 2.73 mmol) at 0° C. was added acetyl chloride (0.1 mL, 1.36 mmol). The reaction was allowed to warm to 25° C. over 19 h. The reaction was then taken up in CH2Cl2 (50 mL) and washed with 1N HCl (5 mL) and water (5 mL). The organics were washed with saturated aqueous sodium chloride (30 mL), dried over MgSO4, filtered and concentrated. The residue was purified with Biotage Flash 40S chromatography, eluting with 1:1 ethyl acetate-hexanes, to provide 1-acetyl-4-[4-(2-methyl-quinolin-4-ylmethoxy)-benzenesulfonylamino]-piperidine-3-carboxylic acid ethyl ester as a white solid (0.6 g, 92%). MS: 526 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595327B2
Source datasetuspto-grants-2009_09
ORD IDord-c5155e53c6b643a1bd480285ff4d3d2e
Source noteuspto-grants-2009_09