HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047373Generated: November 2, 2026
Chloroacetyl chloride → HCID 178521454, compound
https://huagongshe.com/reaction/1047373
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | 4-(2,4-Difluorophenyl)piperidine | HCID 16679314 | — |
| Reactant | 2-Chloro-1-[4-(2,4-difluoro-phenyl)-piperidin-1-yl]-ethanone | HCID 58118169 | — |
| Reactant | HCID 178526690 | HCID 178526690 | — |
| Product | HCID 178521454 | HCID 178521454 | — |
Reaction Steps
1-[4-(2,4-Difluoro-phenyl)-piperidin-1-yl]-2-[trans-4-(4-nitro-3-trifluoromethyl-phenylamino)-cyclohexyloxy]-ethanone was prepared using a two-step synthesis. In the first step, 1-chloracetyl-4-(2,4-difluoro-phenyl)-piperidine (also known as 2-chloro-1-[4-(2,4-difluoro-phenyl)-piperidin-1-yl]-ethanone) was prepared from 4-(2,4-difluoro-phenyl)-piperidine and chloroacetyl chloride using the procedure illustrated in Example 4. In the second step, the 1-[4-(2,4-difluoro-phenyl)-piperidin-1-yl]-2-[trans-4-(4-nitro-3-trifluoromethyl-phenylamino)-cyclohexyloxy]-ethanone was prepared from the 1-chloracetyl-4-(2,4-difluoro-phenyl)-piperidine and trans-4-(4-nitro-3-trifluoromethyl-phenylamino)-cyclohexanol (prepared in accordance with Example 5) using the procedure illustrated in Example 11. This afforded the product as a yellow solid (16% yield). The structure was confirmed using Protocol II-A. Calculated mass=542; observed mass=543; HPLC retention time=4.36 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569495B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-b88b5cbc745749308e683499e28aa51c |
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| Source note | uspto-grants-2013_10 |
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