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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398842Generated: October 27, 2026

Methyl 3-amino-4-chloro-2-((3-hydroxypropyl)amino]benzoate → Methyl 4-chloro-2-[(3-hydroxypropyl)amino]-3-{[(6-methoxy-4-methylpyridin-3-yl)carbamothioyl]amino}benzoate

https://huagongshe.com/reaction/1398842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-amino-4-chloro-2-((3-hydroxypropyl)amino]benzoateHCID 68739849—
Reactant5-Isothiocyanato-2-methoxy-4-methylpyridineHCID 86632884—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-chloro-2-[(3-hydroxypropyl)amino]-3-{[(6-methoxy-4-methylpyridin-3-yl)carbamothioyl]amino}benzoateHCID 86632883—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of methyl 3-amino-4-chloro-2-[(3-hydroxypropyl)amino]benzoate (4.00 g, 15.5 mmol) and 5-isothiocyanato-2-methoxy-4-methylpyridine (8.36 g, 46.4 mmol) in tetrahydrofuran (30 mL) was stirred at 70° C. for 8 hr. The mixture was concentrated in vacuo, and the residue was purified by flash column chromatography on silica gel eluting with a 50-100% ethyl acetate/n-hexane gradient mixture. The filtrate was concentrated in vacuo to give methyl 4-chloro-2-[(3-hydroxypropyl)amino]-3-{[(6-methoxy-4-methylpyridin-3-yl)carbamothioyl]amino}benzoate as a brown amorphous (3.90 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901141B2
Source datasetuspto-grants-2014_12
ORD IDord-d879ae1877ee4f578e5913816f9f1912
Source noteuspto-grants-2014_12