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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731771Generated: October 31, 2026

Acetyl chloride → 2-[(5-Acetylamino-2-pyridinyl)thio]ethyl-3-chlorobenzoate

https://huagongshe.com/reaction/731771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant2-[(5-Amino-2-pyridinyl)thio]ethyl-3-chlorobenzoateHCID 57838108—
SolventDichloromethaneHCID 6344—
Product2-[(5-Acetylamino-2-pyridinyl)thio]ethyl-3-chlorobenzoateHCID 57838115—

Reaction Steps

A mixture of 2-[(5-nitro-2-pyridinyl)thio]ethyl 3-chlorobenzoate (5) (0.24 g, 0.71 mmol) and 10% Pd/C (0.10 g) in toluene or methanol was agitated under a hydrogen atmosphere (40 PSI) for 1 h. The reaction mixture was filtered through Celite® and concentrated to give 2-[(5-amino-2-pyridinyl)thio]ethyl-3-chlorobenzoate (51), LCMS: purity: 99%; MS (m/e): 309 (MH+), which was used without further purification. Acetyl chloride (4.6 μL, 0.064 mmol) was added to a room temperature solution of 2-[(5-amino-2-pyridinyl)thio]ethyl-3-chlorobenzoate (51) (18.9 mg, 0.061 mmol) and triethylamine (18 μL, 0.13 mmol) in anhydrous dichloromethane (1.0 mL), After 16 h, the reaction mixture was diluted with dichloromethane and washed with 1N HCl and brine and then dried over anhydrous MgSO4. Purification by silica gel chromatography provided 2-[(5-acetylamino-2-pyridinyl)thio]ethyl-3-chlorobenzoate (52), LCMS: purity: 99%; MS (m/e): 351 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585883B2
Source datasetuspto-grants-2009_09
ORD IDord-55b648b2a91b4266bfc81d485d1567a8
Source noteuspto-grants-2009_09