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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Azanium;hydrate | HCID 22024077 | — |
| Reactant | HCID 67169759 | HCID 67169759 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(tert-Butyl)-5-(4-(4-chlorophenoxy)piperidine-1-carbonyl)benzamide | HCID 67168242 | 35% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051296B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-05d6885f07b44654aedb7be985f46c0c |
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| Source note | uspto-grants-2015_06 |
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