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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893240Generated: November 1, 2026

Trifluoroacetic acid → HCID 49763930, compound

https://huagongshe.com/reaction/1893240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 49763929HCID 49763929—
ProductHCID 49763930HCID 49763930—

Reaction Steps

N-[(1-{4-[4-(3-tert-Butyl-ureido)-phenyl]-cyclohexyl}-azetidin-3-ylcarbamoyl)-methyl]-3-trifluoromethyl-benzamide (prepared as described in Example 18, 50 mg, 0.087 mmol) was treated with TFA (1 mL) at room temperature overnight. The reaction was quenched with saturated NaHCO3. The reaction solution was extracted with a chloroform/IPA “cocktail” (˜3:1, v/v). The organic layer was dried over anhydrous Na2SO4, filtered and concentrated to give the crude product, which was then purified by a CombiFlash® system using ethyl acetate and 7N NH3 in MeOH as eluent (from pure ethyl acetate to 5% 7N NH3 in MeOH in ethyl acetate) to afford two title compound as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513229B2
Source datasetuspto-grants-2013_08
ORD IDord-d27d197c6756454ea8e8c78bc0c61084
Source noteuspto-grants-2013_08