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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888382Generated: October 30, 2026

Dichloromethane → Methyl 3-[(methylamino)carbonothioyl]-5-(5-methylpyridin-2-yl)benzoate

https://huagongshe.com/reaction/888382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantLawesson's reagentHCID 87949—
ReactantMethyl 3-[(methylamino)carbonyl]-5-(5-methylpyridin-2-yl)benzoateHCID 68496788—
Solvent1,1-DichloroethaneHCID 6365—
ProductMethyl 3-[(methylamino)carbonothioyl]-5-(5-methylpyridin-2-yl)benzoateHCID 86646758112.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of methyl 3-[(methylamino)carbonyl]-5-(5-methylpyridin-2-yl)benzoate (2.90 g, 10.2 mmol) in dichloroethane (20 mL) was added 2,4-bis-(4-methoxyphenyl)-1,3-dithia-2,4-diphosphetane 2,4-disulfide (Lawesson's reagent) (2.27 g, 5.61 mmol) and the mixture heated to 60° C. After 2 h, the reaction was cooled to ambient temperature. Dichloromethane (200 mL) was added, and the mixture washed with 100 mL of saturated aqueous sodium bicarbonate (2×) and brine (100 mL). The combined organic extracts were dried over sodium sulfate, filtered and concentrated. The residue was purified by silica gel chromatography (100% dichloromethane→90% dichloromethane/methanol) to give the title compound (1.9 g). MS 301.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247401B2
Source datasetuspto-grants-2012_08
ORD IDord-489f178967c74f31a6286d3efdce309d
Source noteuspto-grants-2012_08