HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294876Generated: October 30, 2026
1,2-Dichloroethane → HCID 23218411, compound
https://huagongshe.com/reaction/2294876
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 2-(3,5-Dichlorophenyl)acetic acid | HCID 6452487 | — |
| Reactant | HCID 21472089 | HCID 21472089 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 23218411 | HCID 23218411 | 34.9% |
Reaction Steps
To a stirring solution of 3-amino-1-(2-propyl)-5-(2,2,2-trifluoroethyl)-1,5-benzodiazepine-2,4-dione (180 mg, 0.57 mmol) in N,N-dimethylformamide (2 mL) was added EDC (131 mg, 0.69 mmol), HOBT (46 mg, 0.34 mmol) and 3,5-dichlorophenylacetic acid (140 mg, 0.69 mmol). The reaction was stirred at room temperature for 2 hours. The reaction was diluted with ethyl acetate (50 mL), then washed with 10% aqueous potassium hydrogen sulfate (25 mL) then saturated aqueous sodium hydrogen carbonate (25 mL) and finally, brine (25 mL). The organic layers were combined, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The residue was chromatographed on silica gel eluting with 25-40% ethyl acetate:hexane to give 100 mg of product which was crystallized from ethyl acetate/hexane to give colorless crystals (70 mg). m.p.=185°-186° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05691331 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-6f8ff5092f194bff8eb7f09107f90ade |
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| Source note | uspto-grants-1997_11 |
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