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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047367Generated: October 30, 2026

Chloroacetyl chloride → HCID 178510005, compound

https://huagongshe.com/reaction/1047367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
Reactant4-(Piperazin-1-yl)benzonitrileHCID 2733995—
Reactant4-(4-(2-Chloroacetyl)piperazin-1-yl)benzonitrileHCID 11777571—
ReactantHCID 178526690HCID 178526690—
ProductHCID 178510005HCID 178510005—

Reaction Steps

4-(4-{2-[Trans-4-(4-nitro-3-trifluoromethyl-phenylamino)-cyclohexyloxy]-acetyl}-piperazin-1-yl)-benzonitrile was prepared using a two-step synthesis. In the first step, 1-chloracetyl-4-(4-benzonitrile)-piperazine (also known as 4-[4-(2-chloroacetyl)-piperazin-1-yl]-benzonitrile) was prepared from 4-(piperazin-1-yl)-benzonitrile and chloroacetyl chloride using the procedure illustrated in Example 4. In the second step, the 4-(4-{2-[trans-4-(4-nitro-3-trifluoromethyl-phenylamino)-cyclohexyloxy]-acetyl]-piperazin-1-yl)-benzonitrile was prepared from the 1-chloracetyl-4-(4-benzonitrile)-piperazine 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 (39% yield). The structure was confirmed using Protocol II-A. Calculated mass=532; observed mass=532; HPLC retention time=4.14 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569495B2
Source datasetuspto-grants-2013_10
ORD IDord-72b5e4de0f84426d8e29b272d614aaad
Source noteuspto-grants-2013_10