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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705596Generated: October 30, 2026

Lawesson's reagent → HCID 57818467, compound

https://huagongshe.com/reaction/705596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
ReactantHCID 57818754HCID 57818754—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 57818467HCID 578184674%

Reaction Conditions

Temperature100 °C

Reaction Steps

N-(5-fluoro-2-(4-fluorobenzyloxy)pyrimidin-4-yl)acetamide (50 mg, 0.42 mmol) was stirred in a Biotage Initiator® microwave vessel with 1,2-dichloroethane (3 mL) and Lawesson's reagent (170 mg, 0.42 mmol). The vessel was heated in a Biotage Initiator® microwave to 100° C. for 5 minutes then cooled room temperature, filtered, and diluted with CH2Cl2. The reaction mixture was then washed brine, and the layers were separated. The organic extract was dried onto silica and purified by flash chromatography. The product-containing fractions were then evaporated to dryness and purified again by reverse-phase HPLC to give 4 mg of N-(5-fluoro-2-(4-fluorobenzyl-oxy)pyrimidin-4-yl)ethanethioamide (4%) as a yellow glass: 1H NMR (CDCl3) δ 9.34 (b, 1H), 8.29 (d, J=3 Hz, 1H), 7.41 (m, 2H), 7.06 (m, 2H), 5.33 (s, 2H), 3.13 (s, 3H); HPLC-MS (ESI): m/z 294 (ES−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174970B2
Source datasetuspto-grants-2015_11
ORD IDord-7b1150089f0541f993dbeed39e52c6d4
Source noteuspto-grants-2015_11