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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951272Generated: November 2, 2026

Thioglycolic Acid → N-Cyclopropyl-3-(2-mercaptoacetamido)-4-methylbenzamide

https://huagongshe.com/reaction/1951272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioglycolic AcidHCID 1133—
Reactant3-Amino-N-cyclopropyl-4-methylbenzamide hydrochlorideHCID 44203194—
SolventTolueneHCID 1140—
ProductN-Cyclopropyl-3-(2-mercaptoacetamido)-4-methylbenzamideHCID 5976141932%

Reaction Steps

A solution of mercaptoacetic acid (1.65 mL, 24.2 mmol) and 5.0 g (22 mmol) of 3-amino-N-cyclopropyl-4-methylbenzamide hydrochloride (prepared as described in WO 04/071440) in toluene (40 mL) was refluxed for 16 h. At this time, an additional 0.8 mL of mercaptoacetic acid was added and the mixture was continued at reflux for an additional 2 days. After cooling to rt, the solid was collected by vacuum filtration and was rinsed with EtOAc (2×50 mL). The resulting solid was then slurried in water (50 mL) and the solid was recollected by vacuum filtration and rinsed with add'n water. The resulting solid was air dried in the funnel then under vacuum overnight to afford 1.86 g (32%) of a white solid as compound a. HPLC Ret time=1.83 min. LCMS [M+H]+ 265.37.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404689B2
Source datasetuspto-grants-2013_03
ORD IDord-d45f80d89f994a5fa9d26640c0f83629
Source noteuspto-grants-2013_03