HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930518Generated: November 2, 2026
Lawesson's reagent → HCID 86652387, compound
https://huagongshe.com/reaction/1930518
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | HCID 24948331 | HCID 24948331 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86652387 | HCID 86652387 | 27.7% |
Reaction Steps
To the solution of 2-chloro-4-[3-(3,5-dichlorophenyl)-3-(trifluoromethyl)pyrrolidin1-yl]-N-(pyridin-2-ylmethyl)benzamide (0.35 g) in toluene was added Lawesson reagent (0.28 g) and the mixture was heated to reflux for 3 hours. After the mixture was cooled to room temperature, the solvent was distilled away under the reduced pressure, and the residue was purified by silica gel chromatography to yield 2-chloro-4-[3-(3,5-dichlorophenyl)-3-(trifluoromethyl)pyrrolidin1-yl]-N-(pyridin-2-ylmethyl)benzenecarbothioamide (0.10 g). 1H-NMR (CDCl3) δ: 2.51-2.61 (1H, m), 2.84-2.92 (1H, m), 3.45-3.61 (2H, m), 3.79 (1H, d), 4.08 (1H, d), 5.08 (2H, d), 6.49-6.54 (2H, m), 7.22-7.28 (3H, m), 7.36 (1H, d), 7.40 (1H, t), 7.72 (1H, td), 7.79 (1H, d), 8.54 (1H, d), 9.27 (1H, br s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188122B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-6787ce8b465940dfb53c200b40e3b71e |
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| Source note | uspto-grants-2012_05 |
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