Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920722Generated: October 26, 2026

Trichloroacetyl chloride → N-(4,5-dimethylisoxazol-3-yl)-4-(tetrahydro-2H-pyran-4-carbonyl)-1,4-diazepane-1-carboxamide

https://huagongshe.com/reaction/1920722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetyl chlorideHCID 6420—
ReactantSodium CarbonateHCID 10340—
ReactantDiisopropylethylamineHCID 81531—
Reactant4,5-Dimethylisoxazol-3-amineHCID 84148—
ReactantSodium BicarbonateHCID 516892—
Reactant(1,4-Diazepan-1-yl)(tetrahydro-2H-pyran-4-yl)methanoneHCID 28776660—
SolventDichloromethaneHCID 6344—
ProductN-(4,5-dimethylisoxazol-3-yl)-4-(tetrahydro-2H-pyran-4-carbonyl)-1,4-diazepane-1-carboxamideHCID 545834564.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 90 mg (0.8 mmol) of 4,5-dimethyl-isoxazol-3-ylamine in DCM (2 mL) was added N,N-diisopropylethylamine (278 μL, 1.6 mmol), followed by 89 μL (0.8 mmol) of trichloroacetylchloride. The reaction mixture was shaken on an orbital shaker for 18 h. Saturated aqueous NaHCO3 solution (3 mL) was added to the reaction mixture. The organic layer was dried over Na2SO4, filtered and the filtrate was concentrated under reduced pressure. The residue was dissolved in DMF (3 mL) and added to 487 mg (0.88 mmol) of [1,4]diazepan-1-yl-(tetrahydro-pyran-4-yl)-methanone (triple trifluoroacetic acid salt). To this solution 339 mg (3.2 mmol) of Na2CO3 were added and the mixture was heated in a sealed tube at 100° C. for 18 h. The reaction was cooled to room temperature, filtered and the filtrate was concentrated under reduced pressure. The residue was purified by mass-triggered preparative LC-MS to afford 12 mg of 4-(tetrahydro-pyran-4-carbonyl)-[1,4]diazepane-1-carboxylic acid (4,5-dimethyl-isoxazol-3-yl)-amide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173638B2
Source datasetuspto-grants-2012_05
ORD IDord-0ad3a3ecde494f789b69a8e19ba90bc6
Source noteuspto-grants-2012_05