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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047373Generated: November 2, 2026

Chloroacetyl chloride → HCID 178521454, compound

https://huagongshe.com/reaction/1047373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
Reactant4-(2,4-Difluorophenyl)piperidineHCID 16679314—
Reactant2-Chloro-1-[4-(2,4-difluoro-phenyl)-piperidin-1-yl]-ethanoneHCID 58118169—
ReactantHCID 178526690HCID 178526690—
ProductHCID 178521454HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569495B2
Source datasetuspto-grants-2013_10
ORD IDord-b88b5cbc745749308e683499e28aa51c
Source noteuspto-grants-2013_10