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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803182Generated: November 1, 2026

Allyl bromide → allyl 2-fluoro-5-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenylcarbamimidothioate, hydrobromide

https://huagongshe.com/reaction/1803182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant1-(2-fluoro-5-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenyl)thioureaHCID 86649890—
SolventEthanolHCID 702—
Productallyl 2-fluoro-5-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenylcarbamimidothioate, hydrobromideHCID 178419557101.4%

Reaction Conditions

Temperature70 °C

Reaction Steps

Step U (1): Allyl bromide (0.308 mL, 3.55 mmol) was added to a solution of 1-(2-fluoro-5-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenyl)thiourea (1.0 g, 3.55 mmol, from Preparation B, Step B(4)) in absolute ethanol (25 mL). The resulting mixture was heated at 70° C. for 2 h. After cooling to rt, the reaction was concentrated in vacuo. The residual volatiles were removed under high vacuum to afford allyl 2-fluoro-5-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenylcarbamimidothioate, hydrobromide (1.45 g, 3.60 mmol, 101% yield) as an off-white solid. LC-MS (M+H)+ 322.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349880B2
Source datasetuspto-grants-2013_01
ORD IDord-6e84a5090af34e3889be05dc6ac69f9c
Source noteuspto-grants-2013_01