HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099090Generated: October 26, 2026
Dichloromethane → 4-methoxy-N-[2-piperidin-1-yl-5-(trifluoromethyl)phenyl]benzamide
https://huagongshe.com/reaction/2099090
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(Piperidin-1-yl)-5-(trifluoromethyl)aniline | HCID 694756 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-methoxy-N-[2-piperidin-1-yl-5-(trifluoromethyl)phenyl]benzamide | HCID 1422797 | — |
Reaction Steps
4-Methoxybenzoyl chloride (250 mg, 1.47 mmol, commercially available product) and triethylamine (254 μl, 1.83 mmol) were sequentially added at 0° C. to a dichloromethane (4 ml) solution of 2-(1-piperidinyl)-5-(trifluoromethyl)aniline (147 mg, 0.602 mmol), obtained as described in Referential Example 1-2. The resulting mixture was warmed to room temperature and stirred for 17 hours. Water was added to the mixture, and the resulting mixture was extracted three times with ethyl acetate. The obtained organic layer was washed with a saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (20 g, hexane/ethyl acetate=5/1). Thus, N-[2-(1-piperidinyl)-5-(trifluoromethyl)phenyl]-4-methoxybenzamide (GIF-0615) (240 mg, quant.) was yielded as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07569536B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-6e6ea2891aa14d67be541d093ce27f50 |
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| Source note | uspto-grants-2009_08 |
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