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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828095Generated: October 30, 2026

2,4,6-Trimethylpyridine → (RS)-ethoxy-(2-oxo-3-phenylmethanesulfonylamino-2H-pyridin-1-yl)-acetic acid ethyl ester

https://huagongshe.com/reaction/1828095

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrimethylpyridineHCID 7953—
ReactantPhenylmethanesulfonyl chlorideHCID 74740—
Reactant(RS)-(3-amino-2-oxo-2H-pyridin-1-yl)-ethoxy-acetic acid ethyl esterHCID 69641593—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(RS)-ethoxy-(2-oxo-3-phenylmethanesulfonylamino-2H-pyridin-1-yl)-acetic acid ethyl esterHCID 6964145884.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred, cooled (0° C.) solution (RS)-(3-amino-2-oxo-2H-pyridin-1-yl)-ethoxy-acetic acid ethyl ester (428 mg) and 2,4,6-collidine (0.47 ml) in THF (3 ml) under an argon atmosphere was added dropwise a solution of alpha-toluenesulphonylchloride (340 mg) in THF (2 ml) over 10 min. When addition was complete, stirring at 0° C. was continued for 2 h. The mixture was diluted with EtOAc, washed with 1.0 N HCl and brine, dried (MgSO4), filtered and concentrated to give (RS)-ethoxy-(2-oxo-3-phenylmethanesulfonylamino-2H-pyridin-1-yl)-acetic acid ethyl ester (592 mg) as light brown solid. MS 393.0 ([M−H]−)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056932B2
Source datasetuspto-grants-2006_06
ORD IDord-58ba4278dc084ec689e6fd4f7f8b661b
Source noteuspto-grants-2006_06