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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803169Generated: November 1, 2026

Methyl iodide → HCID 178504008, compound

https://huagongshe.com/reaction/1803169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1-(3-fluoro-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenyl)thioureaHCID 86649918—
SolventEthanolHCID 702—
ProductHCID 178504008HCID 17850400898.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

Step Q (3): Iodomethane (1.43 mL, 22.9 mmol) was added to a solution of 1-(3-fluoro-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenyl)thiourea (5.48 g, 21.8 mmol) in absolute ethanol (200 mL). The resulting mixture was heated at 70° C. for 3 h. After cooling to rt, the reaction was chilled at −20° C. for 2 h. The precipitate was collected by vacuum filtration. The solid was dried under high vacuum to afford methyl 3-fluoro-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenylcarbamimidothioate, hydroiodide (8.40 g, 21.4 mmol, 98% yield) as an off-white solid. LC-MS (M+H)+ 266.1. 1H NMR (500 MHz, DMSO-d6) δ ppm 8.91 (d, J=2.4 Hz, 1 H), 7.91 (t, J=8.5 Hz, 1 H), 7.64 (dd, J=11.7, 2.0 Hz, 1 H), 7.35 (d, J=7.3 Hz, 1 H), 2.70 (s, 3 H), 2.38 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349880B2
Source datasetuspto-grants-2013_01
ORD IDord-b71ccf3c8c524d5d9e36b983693e5490
Source noteuspto-grants-2013_01