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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092224Generated: November 1, 2026

2-Chloro-6-methylpyridine-4-carbonyl chloride → 1-(2-Chloro-6-methyl-pyridine-4-carbonyl)-3-(3-fluoro-5-methoxy-phenyl)thiourea

https://huagongshe.com/reaction/2092224

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-6-methylpyridine-4-carbonyl chlorideHCID 2782130—
Reactant3-Fluoro-5-methoxyanilineHCID 40427890—
ReactantHCID 178514171HCID 178514171—
SolventAcetoneHCID 180—
Product1-(2-Chloro-6-methyl-pyridine-4-carbonyl)-3-(3-fluoro-5-methoxy-phenyl)thioureaHCID 59455895—

Reaction Steps

2-Chloro-6-methyl-4-pyridinecarbonyl chloride (44.087 g, 0.232 mol) in acetone (1 l) was treated with ammonium isothiocyanate (21.192 g, 0.278 mol) and the mixture was stirred for 1 hour at room temperature. Subsequently, a solution of 3-fluoro-5-methoxybenzenamine (36.02 g, 0.255 mol) in acetone (200 ml) was added dropwise and the reaction mixture was stirred for 4 hours at room temperature. The solvent was evaporated in vacuo and the residue was dissolved in CH2Cl2 (1 l). This organic solution was washed (H2O), dried (MgSO4), filtered and the solvent was evaporated in vacuo to yield a brown solid. The brown solid was triturated in acetonitrile (0.8 l), stirred overnight and the solid was filtered off and dried (vacuum oven, 4 hours at 65° C.). Yield: 59.69 g of intermediate D13 (73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440701B2
Source datasetuspto-grants-2013_05
ORD IDord-c5486371947940ef86f860c85eecbd7a
Source noteuspto-grants-2013_05