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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608816Generated: November 1, 2026

3-(Trifluoromethyl)benzenesulfonyl chloride → HCID 20085682, compound

https://huagongshe.com/reaction/1608816

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2733250—
ReactantHCID 20085642HCID 20085642—
ProductHCID 20085682HCID 2008568287.1%

Reaction Steps

The titled compound was prepared substantially in accordance with the method set forth in Example 1C using 4.84 g (0.0198 mol) of 2-amino-N-[2-(1-methyl-1H-imidazol-2-yl)ethyl]benzamide (prepared in a similar manner as the compound in Example 6A) and 5.25 g (0.0215 mol) of m-trifluoromethylbenzenesulfonyl chloride. After reducing the organic layer to dryness, the resulting yellow solid was recrystallized from an ethyl acetate/diethyl ether solution to provide 7.8 g of the desired titled compound (m.p. 127°-129° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05397798
Source datasetuspto-grants-1995_03
ORD IDord-15e36523dc39452c8bc38b2fd5bf0931
Source noteuspto-grants-1995_03