HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945418Generated: November 2, 2026
1,2-Dichloroethane → HCID 16124990, compound
https://huagongshe.com/reaction/1945418
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Pyridineethanamine | HCID 83275 | — |
| Reactant | HCID 5124065 | HCID 5124065 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 16124990 | HCID 16124990 | 40% |
Reaction Steps
To a solution of 3-[2-(4-adamantan-1-yl-phenoxy)-acetylamino]-benzoic acid (50 mg, 0.123 mmol), 4-(2-aminoethyl)pyridine (22.59 mg, 0.184 mmol) and DIPEA (23.90 mg, 0.184 mmol) in DMF 1 mL was added EDC (35.45 mg, 0.184 mmol) and HOBt (24.99 mg, 0.184 mmol) at room temperature and continued stirring for 16 h at room temperature. Reaction mixture was diluted with ethyl acetate and sequentially washed with aqueous sodium bicarbonate, brine and water, and dried over MgSO4. The solvent was filtered and evaporated under reduced pressure to afford a crude solid, which was purified by column chromatography on silica gel (n-Hexane:EtoAC=1:5) to give 3-[2-(4-adamantan-1-yl-phenoxy)-acetylamino]-N-(2-pyridine-4-yl-ethyl)benzamide as a colorless crystal (25 mg, 40% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394799B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-b7f83bf7a8024c2dbdf8e6165a426a44 |
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| Source note | uspto-grants-2013_03 |
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