HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335613Generated: October 29, 2026
1,2-Dichloroethane → HCID 68431784, compound
https://huagongshe.com/reaction/335613
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 7-Cyanobenzo[b]thiophene-2-carboxylic acid | HCID 59341427 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68431784 | HCID 68431784 | — |
Reaction Steps
1.5 g (7.38 mmol) of 7-cyano-1-benzothiophene-2-carboxylic acid and 1.47 g (7.38 mmol) of R-3-aminoquinuclidine dihydrochloride are initially charged in 25 ml of DMF. At 0° C., 1.70 g (8.86 mmol) of EDC, 1.20 g (8.86 mmol) of HOBt and 3.70 ml (26.6 mmol) of triethylamine are added to the solution. The mixture is stirred at RT for 18 h. The reaction is terminated by addition of a 10% strength aqueous sodium bicarbonate solution, and ethyl acetate is added. The resulting precipitate is filtered off with suction. The mother liquor is extracted twice with ethyl acetate. The organic phases are combined and concentrated. The crude product is purified by silica gel column chromatography (mobile phase: dichloromethane/methanol/25% ammonia 100:20:4). The product fractions are concentrated, dissolved in a mixture of methanol and 1N hydrochloric acid, then again concentrated and dried under high vacuum. 655.1 mg (24.5% of theory) of the title compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08884017B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-729dfb1ef0104df8b0bae89ad9e1a05b |
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| Source note | uspto-grants-2014_11 |
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