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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloro-6-methylpyridine-4-carbonyl chloride | HCID 2782130 | — |
| Reactant | 3-Fluoro-5-methoxyaniline | HCID 40427890 | — |
| Reactant | HCID 178514171 | HCID 178514171 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-(2-Chloro-6-methyl-pyridine-4-carbonyl)-3-(3-fluoro-5-methoxy-phenyl)thiourea | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08440701B2 |
|---|
| Source dataset | uspto-grants-2013_05 |
|---|
| ORD ID | ord-c5486371947940ef86f860c85eecbd7a |
|---|
| Source note | uspto-grants-2013_05 |
|---|