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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601158Generated: October 30, 2026

Triethylamine → Ethyl 2-[(benzyloxy)(3-ethoxy-3-oxopropanoyl)amino]nicotinate

https://huagongshe.com/reaction/601158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl 2-[(benzyloxy)amino]nicotinateHCID 59224790—
ReactantMonoethyl chloromalonateHCID 86592122—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-[(benzyloxy)(3-ethoxy-3-oxopropanoyl)amino]nicotinateHCID 8659212165%

Reaction Steps

A solution of the product of Example 157A (1.2 g, 4.4 mmol) and triethylamine (0.49 g, 4.8 mmol) in dichloromethane (25 mL) was treated dropwise with ethyl chloromalonate (0.73 g, 4.8 mmol), stirred for 2 hr and partitioned between ethyl acetate and water and the layers were separated. The ethyl acetate layer was washed with brine, dried (Na2SO4), and concentrated. The residue was purified by column chromatography on silica gel eluting with hexane and ethyl acetate (3:1) to provide the title compound (1.1 g, 65%). MS (DCI) m/z 387 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902203B2
Source datasetuspto-grants-2011_03
ORD IDord-efd6d4300000405dacf9ea1030a7a911
Source noteuspto-grants-2011_03