HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648506Generated: November 1, 2026
Dichloromethane → HCID 86742082, compound
https://huagongshe.com/reaction/648506
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 13603946 | HCID 13603946 | — |
| Reactant | HCID 13825050 | HCID 13825050 | — |
| Product | HCID 86742082 | HCID 86742082 | — |
Reaction Steps
4-[[7-(Trifluoromethyl)-4-quinolyl]amino]benzoyl chloride hydrochloride (0.69 g) was added slowly to a stirred mixture of 4-[(2-pyridyl)sulfinyl]piperidine hydrochloride (0.50 g) and triethylamine (1.72 ml) in dry methylene chloride (22 ml) at room temperature. The resultant mixture was stirred at the same temperature for 1.5 hours and concentrated in vacuo. The residue was partitioned between chloroform and water. The organic layer was washed with saturated aqueous sodium bicarbonate, dried over magnesium sulfate, and concentrated to dryness in vacuo. The resultant crystalline residue was recrystallized from a mixture of methylene chloride and methanol and washed successively with methanol and methylene chloride to give 4-[(2-pyridyl(sulfinyl]-1-[4-[[7-(trifluoromethyl)-4-quinolyl]amino]benzoyl]piperidine (0.59 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04735952 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-c67dc822dd1943519f0bae8251ebd547 |
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| Source note | uspto-grants-1988_04 |
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