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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047141Generated: November 1, 2026

Lawesson's reagent → AZD7118 Bromo Thioamide

https://huagongshe.com/reaction/1047141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
ReactantAZD7118 Bromo AmideHCID 59208425—
SolventTetrahydrofuranHCID 8028—
ProductAZD7118 Bromo ThioamideHCID 5920843977%

Reaction Conditions

Temperature70 °C

Reaction Steps

A suspended mixture of 5-bromo-2-(3-ethylureido)isonicotinamide (Intermediate 5, 237 g, 830 mmol), Lawesson's Reagent (336 g, 830 mmol), and tetrahydrofuran (3 L) was stirred at 70° C. for 18 h. The precipitate was collected by filtration and washed with methyl tert-butyl ether (2×500 L). This solid was then dried in the vacuum oven at 50° C. for 12 h to give 192 g (77%) of 5-bromo-2-(3-ethylureido)pyridine-4-carbothioamide as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569484B2
Source datasetuspto-grants-2013_10
ORD IDord-2f6881b60487450b9c0111a99f6f0781
Source noteuspto-grants-2013_10