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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920729Generated: October 31, 2026

Trichloroacetyl chloride → 4-(Tetrahydro-pyran-4-carbonyl)-[1,4]diazepane-1-carboxylic acid (5-sec-butyl-pyridin-2-yl)-amide

https://huagongshe.com/reaction/1920729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetyl chlorideHCID 6420—
ReactantSodium CarbonateHCID 10340—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Sec-butyl-pyridin-2-ylamineHCID 20674669—
Reactant(1,4-Diazepan-1-yl)(tetrahydro-2H-pyran-4-yl)methanoneHCID 28776660—
SolventDichloromethaneHCID 6344—
Product4-(Tetrahydro-pyran-4-carbonyl)-[1,4]diazepane-1-carboxylic acid (5-sec-butyl-pyridin-2-yl)-amideHCID 591433809%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 90 mg (0.6 mmol) of 5-sec-butyl-pyridin-2-ylamine in DCM (2 mL) was added N,N-diisopropylethylamine (348 μL, 1.2 mmol), followed by 67 μL (0.6 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 (2 mL) and added to 332 mg (0.6 mmol) of [1,4]diazepan-1-yl-(tetrahydro-pyran-4-yl)-methanone (triple trifluoroacetic acid salt). To this solution 254 mg (2.4 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 21 mg of 4-(tetrahydro-pyran-4-carbonyl)-[1,4]diazepane-1-carboxylic acid (5-sec-butyl-pyridin-2-yl)-amide. ES−MS: m/z 389;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173638B2
Source datasetuspto-grants-2012_05
ORD IDord-5c04c501a01846e58284b4dd33d0f5fc
Source noteuspto-grants-2012_05