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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188585Generated: October 27, 2026

2,5-Hexanedione → N-({1-[4-(2,5-Dimethyl-pyrrol-1-yl)-cyclohexyl]-azetidin-3-ylcarbamoyl}-methyl)-3-trifluoromethyl-benzamide

https://huagongshe.com/reaction/2188585

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-HexanedioneHCID 8035—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-{[1-(4-Amino-cyclohexyl)-azetidin-3-ylcarbamoyl]-methyl}-3-trifluoromethyl-benzamide TFA saltHCID 86646662—
SolventMethanolHCID 887—
ProductN-({1-[4-(2,5-Dimethyl-pyrrol-1-yl)-cyclohexyl]-azetidin-3-ylcarbamoyl}-methyl)-3-trifluoromethyl-benzamideHCID 49763450—

Reaction Steps

To a solution of N-{[1-(4-amino-cyclohexyl)-azetidin-3-ylcarbamoyl]-methyl}-3-trifluoromethyl-benzamide trifluoroacetic acid salt (as prepared in Example 35 Step B, 0.24 g, 0.4 mmol) in methanol (2 mL) was added DIEA (Aldrich, 0.21 mL, 1.2 mmol) and acetonylacetone (Aldrich, 0.06 mL, 0.5 mmol). The resulting mixture was stirred at rt overnight and the volatile organics were removed by evaporation. The residue was dissolved in water, extracted with EtOAc, dried over Na2SO4. Filtration and evaporation gave a crude product, which was purified by column chromatography (eluent: EtOAc) to give the cis isomer as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324186B2
Source datasetuspto-grants-2012_12
ORD IDord-9dc4365154694580964d35faf067200e
Source noteuspto-grants-2012_12