HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397191Generated: October 28, 2026
Triethylamine → Rac-2-cyclopentyloxy-2-(3,4-dichloro-phenyl)-n-pyridin-2-yl-acetamide
https://huagongshe.com/reaction/397191
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | 2,4,6-Trichlorobenzoyl chloride | HCID 2733703 | — |
| Reactant | Rac-cyclopentyloxy-(3,4-dichloro-phenyl)-acetic acid | HCID 12044174 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Rac-2-cyclopentyloxy-2-(3,4-dichloro-phenyl)-n-pyridin-2-yl-acetamide | HCID 9947241 | 77.3% |
Reaction Steps
A solution of rac-cyclopentyloxy-(3,4-dichloro-phenyl)-acetic acid (from Example 1, 50 mg, 0.17 mmol) and triethylamine (0.07 mL, 0.52 mmol) in toluene (5 mL), previously cooled to 0° C. was treated with 2,4,6-trichlorobenzoyl chloride (0.03 mL, 0.19 mmol) and the mixture was stirred at 0° C. After 1 h, 2-aminopyridine (20 mg, 0.21 mmol) and 4-dimethylaminopyridine (5 mg, 0.035 mmol) were added and the stirring was continued for 1 h at 0° C. The reaction was checked for completion, then it was diluted with water (10 mL) and extracted with dichloromethane (3×10 mL). The combined organic extracts were dried over sodium sulfate, filtered and concentrated in vacuo. The product was purified by chromatography (Biotage Flash 12M column, 80/20 hexanes/ethyl acetate) to give rac-2-cyclopentyloxy-2-(3,4-dichloro-phenyl)-N-pyridin-2-yl-acetamide (48 mg, 76% yield) as a white foam: EI-HRMS m/e calculated for C18H18N2O2Cl2 (M+) 364.0745, found 364.0746.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06608218B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-3e343e133930445fb76d5cf9aaf1bcec |
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| Source note | uspto-grants-2003_08 |
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