HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174037Generated: October 31, 2026
Hydrochloric Acid → HCID 178470773, compound
https://huagongshe.com/reaction/2174037
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 86701658 | HCID 86701658 | — |
| Reactant | HCID 86701659 | HCID 86701659 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178470773 | HCID 178470773 | — |
Reaction Steps
HCl in dioxane (4 M, 2.28 mL, 9.13 mmol) was added to a solution of a mixture of (±)-ethyl 2-(5-cyano-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-benzo[d]imidazol-2-yl)-2-(5,7-dimethyl-1-tosyl-1H-indol-4-yl)acetate and (±)-ethyl 2-(6-cyano-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-benzo[d]imidazol-2-yl)-2-(5,7-dimethyl-1-tosyl-1H-indol-4-yl)acetate (600 mg, 0.913 mmol) in EtOH (12 mL) at room temperature. The resulting mixture was stirred at 60° C. overnight then partitioned between EtOAc and sat. aq. NaHCO3. The aqueous layer was extracted with EtOAc. The combined organics were washed with brine, dried, and concentrated to give the title compound. The residue was taken onto the next step without further purification. MS (ESI+) m/z 527.3 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09056874B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-0f5aff4beffe4e56b797f1738fb7acb3 |
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| Source note | uspto-grants-2015_06 |
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