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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170858Generated: November 3, 2026

1,2-Dichloroethane → 3-(tert-Butyl)-5-(4-(4-chlorophenoxy)piperidine-1-carbonyl)benzamide

https://huagongshe.com/reaction/2170858

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantAzanium;hydrateHCID 22024077—
ReactantHCID 67169759HCID 67169759—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-(tert-Butyl)-5-(4-(4-chlorophenoxy)piperidine-1-carbonyl)benzamideHCID 6716824235%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of 3-(tert-butyl)-5-(4-(4-chlorophenoxy)piperidine-1-carbonyl)benzoic acid (30 mg, 0.072 mmol, Step-1), EDC (21 mg, 0.11 mmol), HOBT (17 mg, 0.11 mmol), and N,N-diisopropylethylamine (0.28 mL, 1.61 mmol) in N,N-dimethylformamide (3 mL) was add 25% ammonium water (1 mL) at room temperature. After stirring at 60° C. for 2 hours, the mixture was poured into water (5 mL). This was extracted with ethyl acetate (5 mL) and washed with water (5 mL). The organic layer was dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica-gel column chromatography (NH-gel, eluting with ethyl acetate) and then preparative LC-MS to give 10.4 mg (35% yield) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051296B2
Source datasetuspto-grants-2015_06
ORD IDord-05d6885f07b44654aedb7be985f46c0c
Source noteuspto-grants-2015_06